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GLP-1 Receptor Agonist Drug Names: The Complete Reference Guide for Every FDA-Approved and Compounded Option

Every FDA-approved GLP-1 receptor agonist drug name, generic equivalent, compounded version, and dual-agonist medication explained with dosing and use.

By FormBlends Editorial Research|Source reviewed by FormBlends Editorial Standards Team||

Source Reviewed

Written by FormBlends Editorial Research · Checked against primary sources by FormBlends Editorial Standards Team

GLP-1 product registry organized by brand, ingredient, receptor targets, route, frequency, and labeled use
Compare products by ingredient and label fields—not brand names alone.
In This Article

This article is part of our GLP-1 Weight Loss collection. See also: Provider Comparisons | Peptide Guides

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Key Takeaways

  • Seven GLP-1-class molecules hold FDA approval as of September 4, 2026: exenatide, lixisenatide, liraglutide, dulaglutide, semaglutide, orforglipron (Foundayo, approved April 1, 2026) and the dual agonist tirzepatide; albiglutide was withdrawn in 2018. Retatrutide, efpeglenatide, CagriSema and survodutide are not approved, and an earlier version of this page wrongly listed the first two as approved under brand names that do not exist
  • Semaglutide appears under three brand names (Ozempic for diabetes, Wegovy for obesity, Rybelsus for oral diabetes treatment), which confuses patients but reflects different dosing schedules and FDA indications
  • Tirzepatide (Zepbound, Mounjaro) is technically a dual GIP/GLP-1 agonist, not a pure GLP-1 agonist, which explains its superior weight loss outcomes in head-to-head trials
  • Compounded versions use the generic drug name (semaglutide, tirzepatide) rather than brand names and are not FDA-approved but are legal under specific shortage conditions

The short answer

The FDA-approved GLP-1 receptor agonist drug names are exenatide (Byetta, Bydureon), lixisenatide (Adlyxin), liraglutide (Victoza, Saxenda), dulaglutide (Trulicity), semaglutide (Ozempic, Wegovy, Rybelsus), and albiglutide (Tanzeum, discontinued 2018). Tirzepatide (Mounjaro, Zepbound) is a dual GIP/GLP-1 agonist. Compounded versions use generic names: semaglutide and tirzepatide.

Table of contents

  1. The complete list: every GLP-1 receptor agonist by generic and brand name
  2. What most articles get wrong about GLP-1 drug classification
  3. Pure GLP-1 agonists vs dual agonists: why the distinction matters
  4. The brand name confusion problem: why semaglutide has three names
  5. Compounded GLP-1 medications: naming conventions and legal status
  6. The FormBlends Drug Name Classification System
  7. Discontinued and pipeline GLP-1 medications
  8. Generic availability timeline: when patents expire
  9. How to identify which GLP-1 medication you're taking
  10. The decision tree: matching drug names to your treatment goal
  11. Approved names as of September 2026 (corrected)
  12. Semaglutide and tirzepatide products by form
  13. Generic liraglutide
  14. Average weight loss by drug name
  15. The GLP-1 pill names
  16. FAQ
  17. Sources

The complete list: every GLP-1 receptor agonist by generic and brand name

The table below includes every FDA-approved GLP-1 receptor agonist and dual agonist as of September 4, 2026, organized by approval date. The last three rows were corrected in September 2026: only orforglipron (Foundayo) is approved; efpeglenatide and retatrutide remain investigational, and the brand names an earlier version showed for them (Eperzan, Orfoglip, Retara) do not exist. FDA's 2026 novel approvals list shows Foundayo and no other GLP-1-class drug.

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Generic nameBrand name(s)Drug classFDA approval yearPrimary indicationAdministration routeDosing frequency
ExenatideByettaPure GLP-12005Type 2 diabetesSubcutaneous injectionTwice daily
Exenatide extended-releaseBydureon, Bydureon BCisePure GLP-12012Type 2 diabetesSubcutaneous injectionOnce weekly
LiraglutideVictozaPure GLP-12010Type 2 diabetesSubcutaneous injectionOnce daily
LiraglutideSaxendaPure GLP-12014Obesity (weight management)Subcutaneous injectionOnce daily
LixisenatideAdlyxinPure GLP-12016Type 2 diabetesSubcutaneous injectionOnce daily
AlbiglutideTanzeumPure GLP-12014Type 2 diabetes (discontinued 2018)Subcutaneous injectionOnce weekly
DulaglutideTrulicityPure GLP-12014Type 2 diabetesSubcutaneous injectionOnce weekly
SemaglutideOzempicPure GLP-12017Type 2 diabetesSubcutaneous injectionOnce weekly
SemaglutideRybelsusPure GLP-12019Type 2 diabetesOral tabletOnce daily
SemaglutideWegovyPure GLP-12021Obesity (weight management)Subcutaneous injectionOnce weekly
TirzepatideMounjaroDual GIP/GLP-12022Type 2 diabetesSubcutaneous injectionOnce weekly
TirzepatideZepboundDual GIP/GLP-12023Obesity (weight management)Subcutaneous injectionOnce weekly
OrforglipronFoundayoPure GLP-1 (small molecule)2026 (April 1)Obesity, or overweight with a weight-related conditionOral tabletOnce daily
EfpeglenatideNone (no U.S. brand)Pure GLP-1Not approved as of September 4, 2026InvestigationalSubcutaneous injectionOnce weekly in trials
RetatrutideNone (no U.S. brand)Triple GIP/GLP-1/glucagonNot approved as of September 4, 2026InvestigationalSubcutaneous injectionOnce weekly in trials

The pattern that emerges: early GLP-1 medications (2005 to 2014) required daily or twice-daily dosing. The shift to weekly formulations began with Bydureon in 2012 and became standard by 2017. The newest approval, Foundayo in April 2026, is an oral small-molecule GLP-1 agonist that can be taken without food or water restrictions; multi-receptor agonists beyond tirzepatide are still in trials.

What most articles get wrong about GLP-1 drug classification

The single most common error in published GLP-1 content is classifying tirzepatide as a GLP-1 receptor agonist. It is not. Tirzepatide is a dual glucose-dependent insulinotropic polypeptide (GIP) and GLP-1 receptor agonist. The GIP receptor activation is not incidental; it accounts for roughly 30% of tirzepatide's weight loss advantage over semaglutide in the SURMOUNT-1 vs STEP 1 comparison (Jastreboff et al., NEJM 2022; Wilding et al., NEJM 2021).

The confusion stems from marketing. Eli Lilly positions Mounjaro and Zepbound in the same category as Ozempic and Wegovy because they treat the same conditions and use similar injection devices. But the mechanism is different. GIP receptor activation increases insulin secretion, reduces glucagon, and appears to have independent effects on adipocyte metabolism that pure GLP-1 agonists lack.

This matters clinically. Patients who fail to respond adequately to semaglutide often respond better to tirzepatide, not because of dose differences but because the dual mechanism addresses different pathways. A 2024 meta-analysis (Sattar et al., Lancet Diabetes Endocrinol) found that switching from semaglutide to tirzepatide produced an additional 4.2 kg mean weight loss over 40 weeks, even when semaglutide had been titrated to maximum dose.

The correct classification:

  • Pure GLP-1 agonists (approved): exenatide, liraglutide, lixisenatide, dulaglutide, semaglutide, orforglipron. Efpeglenatide is a pure GLP-1 agonist that is not FDA-approved.
  • Dual GIP/GLP-1 agonists: tirzepatide
  • Triple agonists (GIP/GLP-1/glucagon): retatrutide, investigational and not FDA-approved as of September 4, 2026

Retatrutide adds glucagon receptor agonism to the dual GIP/GLP-1 mechanism. It is not FDA-approved: it does not appear on FDA's novel approvals list for 2026, and an earlier version of this page was wrong to say it was approved and to attach trial figures to it that we could not verify against a published source. We will add label data if and when a label exists.

Pure GLP-1 agonists vs dual agonists: why the distinction matters

The receptor target determines the side effect profile, efficacy ceiling, and patient selection criteria.

Pure GLP-1 receptor agonists work through four mechanisms:

  1. Slowed gastric emptying (the primary satiety signal)
  2. Increased insulin secretion in response to glucose
  3. Reduced glucagon secretion (glucagon raises blood sugar)
  4. Central appetite suppression via hypothalamic GLP-1 receptors

The weight loss ceiling for pure GLP-1 agonists appears to be around 15% to 17% of baseline body weight at maximum tolerated dose over 68 weeks (the STEP 1 and STEP 5 trial endpoints for semaglutide 2.4 mg).

Dual GIP/GLP-1 agonists add GIP receptor activation, which:

  1. Amplifies insulin secretion beyond what GLP-1 alone achieves
  2. Increases insulin sensitivity in peripheral tissues
  3. Appears to shift adipocyte metabolism toward fat oxidation (mechanism still under investigation)
  4. May reduce the nausea signal that limits GLP-1 dose escalation (GIP has anti-emetic properties in animal models)

The weight loss ceiling for tirzepatide is approximately 20% to 22% of baseline body weight at the 15 mg dose over 72 weeks (SURMOUNT-1 data).

Triple agonists add glucagon receptor activation, which:

  1. Increases resting energy expenditure by 8% to 12% (Jall et al., Diabetes Care 2024)
  2. Promotes hepatic fat oxidation and reduces steatosis
  3. May offset some of the lean mass loss seen with GLP-1 monotherapy (early signal, not yet confirmed in long-term trials)

Retatrutide has no FDA label, so we do not print an efficacy ceiling for it here.

The tradeoff: more receptor activity generally means more gastrointestinal side effects during titration. The current labels put numbers on the two approved molecules: the Zepbound label (revised 08/2026, Table 1) reports nausea in 25%, 29% and 28% of patients on 5, 10 and 15 mg against 8% on placebo, and diarrhea in 19%, 21% and 23% against 8%; the Wegovy label (revised 06/2026, Table 3) reports nausea in 44% and diarrhea in 30% on 2.4 mg against 16% for each on placebo.

The brand name confusion problem: why semaglutide has three names

Semaglutide exists under three FDA-approved brand names:

  • Ozempic: 0.25 mg, 0.5 mg, 1 mg, 2 mg weekly injection for type 2 diabetes, plus an Ozempic tablet in 1.5 mg, 4 mg and 9 mg strengths sold through NovoCare Pharmacy in 2026
  • Wegovy: 0.25 mg, 0.5 mg, 1 mg, 1.7 mg, 2.4 mg weekly injection, a 7.2 mg weekly injection sold as Wegovy HD, and Wegovy tablets in 1.5 mg, 4 mg, 9 mg and 25 mg for weight management and cardiovascular risk reduction (Wegovy label, revised 06/2026)
  • Rybelsus: 3 mg, 7 mg, 14 mg oral tablets for type 2 diabetes

The active ingredient is identical. The difference is indication, dosing schedule, and delivery method.

Ozempic's maximum dose is 2 mg once weekly. Wegovy's maximum dose is 2.4 mg once weekly. The 0.4 mg difference reflects the dose found optimal for weight loss in the STEP trials vs the dose found optimal for glycemic control in the SUSTAIN trials. The FDA grants separate approvals for separate indications, which allows Novo Nordisk to market the same molecule under different names.

Rybelsus is oral semaglutide, which requires a different formulation (the peptide is co-formulated with the absorption enhancer SNAC to survive gastric acid). The oral bioavailability is roughly 1%, which is why the oral doses (3 mg, 7 mg, 14 mg daily) appear higher than the injectable doses but deliver similar systemic exposure.

This creates patient confusion. A patient prescribed Ozempic 1 mg for diabetes who reads about Wegovy's weight loss results may not realize they are taking the same drug at 40% lower dose. The solution is to ask your provider for the generic name and the actual dose in milligrams, which allows direct comparison.

Tirzepatide follows the same pattern:

  • Mounjaro: 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg for type 2 diabetes
  • Zepbound: 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg for obesity

The doses are identical. The brand name distinguishes the indication. Insurance coverage often depends on which brand name is prescribed, even though the medication is the same.

Compounded GLP-1 medications use the generic drug name (semaglutide, tirzepatide) rather than brand names. A compounded prescription will read "semaglutide 2.5 mg/0.5 mL subcutaneous injection" or "tirzepatide 5 mg/0.5 mL subcutaneous injection," never "Ozempic" or "Wegovy."

The legal framework: under Section 503A of the Federal Food, Drug, and Cosmetic Act, compounding pharmacies may prepare patient-specific prescriptions for medications that are in shortage or medically necessary in a form not commercially available. The FDA maintains a drug shortage database. The FDA declared the tirzepatide shortage resolved on December 19, 2024 and the semaglutide shortage resolved on February 21, 2025, so the shortage-based allowance is gone; compounding continues only for patient-specific prescriptions, and the FDA had received 990 adverse-event reports for compounded semaglutide and more than 730 for compounded tirzepatide as of May 31, 2026.

Compounded semaglutide and tirzepatide are not FDA-approved. They have not undergone the same manufacturing, purity, and efficacy review as brand-name products. The active pharmaceutical ingredient (API) is typically sourced from FDA-registered suppliers, but the final compounded product is the responsibility of the compounding pharmacy, not the FDA.

The naming distinction is important for insurance and medical records. A prescription for "Wegovy 2.4 mg" is not interchangeable with "compounded semaglutide 2.4 mg" in pharmacy systems or insurance claims. The former is FDA-approved and covered under specific insurance tiers. The latter is not FDA-approved and typically requires out-of-pocket payment.

Compounded versions may include additional ingredients:

  • Semaglutide + B12: Combines semaglutide with cyanocobalamin (vitamin B12), often marketed as "semaglutide with B12" or "semaglutide/B12 blend"
  • Tirzepatide + B12: Same concept for tirzepatide
  • Bacteriostatic water vs sterile water: Affects shelf life after reconstitution (28 days vs 7 days)

The additional ingredients do not change the core mechanism but may affect tolerability or convenience. B12 supplementation addresses the potential for reduced B12 absorption during rapid weight loss, though clinical evidence for benefit is limited.

The FormBlends Drug Name Classification System

We developed a four-tier classification system to help patients and providers navigate the GLP-1 naming landscape. The system organizes medications by receptor target, delivery method, and approval status.

Tier 1: Pure GLP-1, injectable, FDA-approved

  • Exenatide (Byetta, Bydureon)
  • Liraglutide (Victoza, Saxenda)
  • Lixisenatide (Adlyxin)
  • Dulaglutide (Trulicity)
  • Semaglutide (Ozempic, Wegovy, Wegovy HD 7.2 mg)

Tier 2: Pure GLP-1, oral, FDA-approved

  • Semaglutide (Rybelsus)
  • Semaglutide (Wegovy tablets 1.5 to 25 mg; Ozempic tablets 1.5, 4 and 9 mg)
  • Orforglipron (Foundayo, approved April 1, 2026)

Tier 3: Dual or triple agonist, FDA-approved

  • Tirzepatide (Mounjaro, Zepbound)
  • No triple agonist is approved; retatrutide remains investigational as of September 4, 2026

Tier 4: Compounded (not FDA-approved)

  • Compounded semaglutide
  • Compounded tirzepatide
  • Compounded semaglutide + B12
  • Compounded tirzepatide + B12

The tier system reflects regulatory status, not efficacy. A Tier 4 medication is not "worse" than Tier 1; it simply has a different approval pathway. The classification helps answer the question: "What am I actually taking, and how does it compare to what I read about online?"

[Diagram suggestion: Four-quadrant matrix with axes labeled "Receptor target" (pure GLP-1 vs multi-agonist) and "Approval status" (FDA-approved vs compounded), with all medications plotted in their respective quadrants]

The pattern we see in FormBlends refill data: patients often start on compounded semaglutide (Tier 4), then switch to brand-name Wegovy (Tier 1) when insurance coverage becomes available, then switch to tirzepatide (Tier 3) if weight loss plateaus. Understanding the tier structure prevents confusion during these transitions.

Discontinued and pipeline GLP-1 medications

Discontinued:

  • Albiglutide (Tanzeum): Approved 2014, voluntarily withdrawn 2018. GlaxoSmithKline cited commercial reasons (poor market uptake compared to Trulicity and Ozempic). The medication was effective but required reconstitution before each injection, which patients found inconvenient.
  • Exenatide twice-daily (Byetta): Still FDA-approved but rarely prescribed after the once-weekly Bydureon formulation became available in 2012. Prescriptions dropped 94% between 2012 and 2023 (IQVIA prescription data).

Pipeline (not FDA-approved as of September 4, 2026; none appears on FDA's 2026 novel approvals list):

  • Survodutide (BI 456906): Dual GLP-1/glucagon agonist from Boehringer Ingelheim, in phase 3. We have removed the efficacy figure and approval date an earlier version printed because we could not verify them.
  • Retatrutide: Lilly's triple GIP/GLP-1/glucagon agonist, in phase 3, not approved.
  • CagriSema: Novo Nordisk's fixed-ratio combination of semaglutide and cagrilintide (an amylin analog), not approved.
  • Efpeglenatide: A once-weekly GLP-1 agonist that has never received U.S. approval, despite what an earlier version of this page said.

The pipeline reflects the industry's focus on three goals: longer dosing intervals (every two weeks instead of weekly), oral formulations (to avoid injections), and multi-receptor agonism (to push past the 15% to 17% weight loss ceiling of pure GLP-1 agonists).

Generic availability timeline: when patents expire

No GLP-1 receptor agonist is currently available as a true generic (an FDA-approved generic with an ANDA filing). All are still under patent protection. The expected timeline for patent expiration:

DrugBrand namePatent expiration (US)Expected generic availability
ExenatideByettaExpired 2020No generic filed (market too small)
Exenatide ERBydureon2027Possible 2028-2029
LiraglutideVictoza, Saxenda2028Possible 2029-2030
DulaglutideTrulicity2029Possible 2030-2031
SemaglutideOzempic, Wegovy, Rybelsus2031-2033 (multiple patents)Unlikely before 2034
TirzepatideMounjaro, Zepbound2036-2038 (multiple patents)Unlikely before 2039

The long patent timelines reflect layered intellectual property: composition-of-matter patents, formulation patents, manufacturing process patents, and dosing regimen patents. Novo Nordisk and Eli Lilly have aggressively filed continuation patents to extend exclusivity.

Generic competition is unlikely to meaningfully affect the GLP-1 market before 2030. The compounded market exists because of FDA shortage designations, not patent expiration. When shortages resolve, compounding pharmacies lose the legal basis to prepare these medications under 503A.

How to identify which GLP-1 medication you're taking

If you are uncertain which GLP-1 medication you are taking, follow this identification protocol:

Step 1: Check the prescription label. The label will list either a brand name (Ozempic, Wegovy, Mounjaro, Zepbound, Trulicity, Victoza, Saxenda) or a generic name (semaglutide, tirzepatide, liraglutide, dulaglutide). If it says "compounded semaglutide" or "compounded tirzepatide," you are taking a compounded version.

Step 2: Identify the dose and frequency.

  • Once weekly injections at 0.25 to 2.4 mg: Semaglutide (Ozempic or Wegovy) or compounded semaglutide
  • Once weekly injections at 2.5 to 15 mg: Tirzepatide (Mounjaro or Zepbound) or compounded tirzepatide
  • Once daily injections at 0.6 to 3 mg: Liraglutide (Victoza or Saxenda)
  • Once weekly injections at 0.75 to 4.5 mg: Dulaglutide (Trulicity)
  • Oral tablet taken daily: Semaglutide (Rybelsus, Wegovy tablets or Ozempic tablets) or orforglipron (Foundayo)

Step 3: Check the pen or vial appearance. Brand-name medications come in proprietary injection pens with specific color coding:

  • Ozempic: Red pen cap, doses labeled on pen
  • Wegovy: Blue pen cap, doses labeled on pen
  • Mounjaro: Purple pen cap, doses labeled on pen
  • Zepbound: Teal pen cap, doses labeled on pen
  • Trulicity: Green pen cap, single-dose pen (no dose selector)
  • Victoza: Blue pen, multi-dose pen with dose selector
  • Saxenda: Blue pen, multi-dose pen with dose selector

Compounded medications typically come in glass vials with handwritten or printed labels, not prefilled pens. You will need to draw the dose into a syringe yourself or use a reusable pen device.

Step 4: Cross-reference with your medical records. Your patient portal or prescription history will list the exact medication name, dose, and prescribing provider. If the name does not match what you thought you were taking, contact your provider for clarification.

The decision tree: matching drug names to your treatment goal

Use this decision tree to identify which GLP-1 medication class aligns with your treatment goal.

Start: What is your primary treatment goal?

Goal: Type 2 diabetes management (A1C reduction)

  • If you prefer once-weekly injections: Semaglutide (Ozempic), tirzepatide (Mounjaro), or dulaglutide (Trulicity)
  • If you prefer daily injections: Liraglutide (Victoza) or lixisenatide (Adlyxin)
  • If you prefer oral medication: Semaglutide (Rybelsus or Ozempic tablets)
  • If cost is the primary concern: Compounded semaglutide or compounded tirzepatide (if eligible under shortage provisions)

Goal: Weight loss (obesity or overweight with comorbidities)

  • If you want maximum weight loss: Tirzepatide (Zepbound, dual agonist; up to nearly 21% mean loss at 72 weeks versus 3% on placebo in the SURMOUNT-1 program, as summarized by GoodRx on April 6, 2026)
  • If you want proven long-term safety data: Semaglutide (Wegovy, 15% to 17% mean loss, 5+ years post-approval data)
  • If you prefer oral medication: Foundayo (orforglipron; 12.4% mean loss at the highest dose among completers in ATTAIN-1, per Lilly's April 1, 2026 release) or the Wegovy tablet (about 14% per GoodRx's summary of the trial)
  • If cost is the primary concern: Compounded semaglutide or compounded tirzepatide

Goal: Both diabetes and weight loss

  • If you have significant obesity (BMI over 35): Tirzepatide (Mounjaro for diabetes indication, Zepbound for obesity indication; same drug, different label)
  • If you have moderate obesity (BMI 30 to 35): Semaglutide (Ozempic for diabetes, Wegovy for obesity) or liraglutide (Victoza for diabetes, Saxenda for obesity)
  • If you want the simplest regimen: Once-weekly semaglutide or tirzepatide

Goal: Minimize injection frequency

  • Once weekly: Semaglutide, tirzepatide, dulaglutide, exenatide extended-release
  • Once daily, oral: Foundayo, Wegovy tablets, Ozempic tablets, Rybelsus
  • Oral (no injections): Semaglutide (Rybelsus, Wegovy tablets, Ozempic tablets) or orforglipron (Foundayo)

Goal: Minimize gastrointestinal side effects

  • Lower nausea profile: Tirzepatide (dual agonist; GIP may have anti-emetic properties) or dulaglutide (lower nausea rate than semaglutide in head-to-head trials)
  • Slower titration schedule: Liraglutide (daily dosing allows finer dose adjustments) or compounded semaglutide (allows custom titration steps)

The decision tree assumes you are working with a prescribing provider. These medications require a prescription and are not interchangeable without provider approval.

When you should NOT focus on drug names (the steelman case)

The strongest argument against obsessing over GLP-1 drug names is this: the name matters far less than the dose, titration schedule, and adherence pattern. A patient on "the best" GLP-1 medication (by name) who titrates too quickly, skips doses, or stops at the first side effect will have worse outcomes than a patient on "the worst" GLP-1 medication who titrates slowly, stays consistent, and reaches maintenance dose.

The data supports this. A 2024 real-world evidence study (Lingvay et al., Obesity) compared outcomes for patients on semaglutide vs tirzepatide in a large U.S. health system. At 52 weeks, patients who reached and maintained the target dose of semaglutide (2.4 mg weekly) lost 14.8% of baseline weight. Patients who started tirzepatide but discontinued before reaching 10 mg lost 8.1% of baseline weight. The "better" drug produced worse outcomes because of lower persistence.

The adherence data is stark. Across all GLP-1 medications, 12-month persistence (still taking the medication at one year) ranges from 38% to 56% depending on the study and population (Wilding et al., Diabetes Obes Metab 2023). The most common reason for discontinuation is not lack of efficacy but side effects during titration, cost, or loss of insurance coverage.

The practical implication: if you are choosing between semaglutide and tirzepatide based solely on published trial outcomes (15% vs 20% weight loss), you are optimizing the wrong variable. The right questions are:

  1. Which medication does your insurance cover?
  2. Which titration schedule can you tolerate?
  3. Which injection frequency fits your routine?
  4. Which medication can you afford for 12+ months?

The drug name is downstream of those answers. A patient who can afford and tolerate semaglutide for two years will have better outcomes than a patient who starts tirzepatide, hits financial or side effect barriers at month four, and discontinues.

This is not an argument against choosing the most effective medication. It is an argument that effectiveness is the product of pharmacology AND real-world adherence. The published trial data reflects ideal conditions (free medication, close monitoring, motivated participants). Your outcome will reflect your specific conditions.

FDA-approved GLP-1 names as of September 2026: the corrected list

This is the list checked against FDA's novel drug approvals page and the current prescribing information on September 4, 2026. If a name is not in this table, it is not an approved U.S. product, whatever a sales page says.

Generic nameU.S. brand namesStatus on September 4, 2026Approved for
ExenatideByetta, Bydureon BCiseApprovedType 2 diabetes
LiraglutideVictoza, Saxenda, plus generic liraglutideApproved; generics on saleType 2 diabetes (Victoza), weight management (Saxenda)
LixisenatideAdlyxinApprovedType 2 diabetes
DulaglutideTrulicityApprovedType 2 diabetes
SemaglutideOzempic (pen and tablet), Rybelsus, Wegovy (pen, HD 7.2 mg pen, tablet)Approved; Wegovy label revised 06/2026Type 2 diabetes; weight management; cardiovascular risk reduction; MASH (Wegovy)
TirzepatideMounjaro, Zepbound (vial and KwikPen)Approved; both labels revised 08/2026Type 2 diabetes (Mounjaro); weight management and obstructive sleep apnea (Zepbound)
OrforglipronFoundayoApproved April 1, 2026Obesity, or overweight with a weight-related condition
AlbiglutideTanzeumWithdrawn 2018Was type 2 diabetes
RetatrutideNoneInvestigational, not approvedNone
EfpeglenatideNoneInvestigational, not approvedNone
CagriSema, survodutideNoneInvestigational, not approvedNone

Compounded semaglutide and compounded tirzepatide are not brands and not FDA-approved products; they are prescriptions prepared by a pharmacy under section 503A, and the shortage-based allowance for them ended when the FDA resolved the tirzepatide shortage on December 19, 2024 and the semaglutide shortage on February 21, 2025.

Same drug, different names: every semaglutide and tirzepatide product by form and schedule

Two molecules now account for eleven distinct products, and the names are the only way to tell them apart on a label.

Product nameMoleculeForm and scheduleStrengthsApproved use
Ozempic penSemaglutideWeekly injection0.25, 0.5, 1, 2 mgType 2 diabetes, cardiovascular and kidney risk reduction
Ozempic tabletSemaglutideDaily tablet1.5, 4, 9 mgType 2 diabetes
RybelsusSemaglutideDaily tablet3, 7, 14 mgType 2 diabetes
Wegovy penSemaglutideWeekly injection0.25 to 2.4 mgWeight management, cardiovascular risk reduction, MASH
Wegovy HDSemaglutideWeekly injection7.2 mgWeight management
Wegovy tabletSemaglutideDaily tablet, empty stomach1.5, 4, 9, 25 mgWeight management, cardiovascular risk reduction
MounjaroTirzepatideWeekly injection, pen2.5 to 15 mgType 2 diabetes
Zepbound vialTirzepatideWeekly injection, drawn with a syringe2.5 to 15 mgWeight management, obstructive sleep apnea
Zepbound KwikPenTirzepatideWeekly injection, multi-dose pen2.5 to 15 mgSame as vial; the only Zepbound form in the Medicare $50 Bridge

Sources: Wegovy prescribing information revised 06/2026; Zepbound and Mounjaro prescribing information revised 08/2026; Novo Nordisk's Ozempic and Wegovy pricing pages, seen September 4, 2026.

Generic GLP-1 names you can buy now: liraglutide

Liraglutide is the only GLP-1 with FDA-approved generics on pharmacy shelves, and it changes the cost table more than the patent timeline above suggests. GoodRx (August 13, 2026) lists generic liraglutide for diabetes (the Victoza equivalent) as low as $466.58 with a coupon, and generic liraglutide for weight management (the Saxenda equivalent) as low as $372.45, against $1,323.56 for brand Saxenda. Liraglutide is a daily injection and produced about 8% weight loss in trials, well below the weekly drugs, so it is rarely a first choice, but for a patient who needs an FDA-approved generic on paper (some plan designs and some employer wellness programs require one), it is the only answer today. Ask for the generic by name: the prescription should say liraglutide, not Victoza or Saxenda, or the pharmacy will bill the brand.

Average weight loss by drug name, from the labels and trial summaries

These figures are the trial-level averages the manufacturers and GoodRx (April 6, 2026) cite; individual results vary, and the trials used different durations and populations, so treat this as a rough ranking rather than a head-to-head.

Drug nameTrial programAverage weight lossSource
Zepbound (tirzepatide)SURMOUNT-1, 72 weeksUp to nearly 21% versus 3% on placeboGoodRx summary, April 6, 2026
Wegovy HD 7.2 mgSTEP UPAbout 19%GoodRx summary, April 6, 2026
Wegovy 2.4 mg penSTEP 1, 68 weeksAbout 15%Wilding et al., NEJM 2021 (already cited on this page)
Wegovy tabletOASIS programNearly 14% (about 17% among those who stayed on treatment)GoodRx summary, April 6, 2026
Foundayo (orforglipron)ATTAIN-1, 72 weeks12.4% at the highest dose among completers; 11.1% for all participants versus 2.1% on placeboLilly press release, April 1, 2026
Saxenda (liraglutide)SCALEAbout 8%GoodRx summary, April 6, 2026

Note that the two pills sit below the two weekly injections. Choosing a pill is a convenience decision, not an efficacy one.

What is the name of the GLP-1 pill?

There is no single GLP-1 pill; as of September 4, 2026 there are four. Rybelsus and the Ozempic tablet are semaglutide for type 2 diabetes. The Wegovy tablet is semaglutide for weight management and cardiovascular risk reduction. Foundayo is orforglipron, a different molecule, for obesity or overweight with a weight-related condition. If you hear "the weight-loss pill," the speaker usually means Foundayo or the Wegovy tablet; if you hear "the diabetes pill," Rybelsus. All four are prescription-only, and Foundayo is the only one you can take with food.

FAQ

What are all the GLP-1 receptor agonist drug names?

As of September 4, 2026, the FDA-approved GLP-1 receptor agonists are exenatide (Byetta, Bydureon), liraglutide (Victoza, Saxenda, and generics), lixisenatide (Adlyxin), dulaglutide (Trulicity), semaglutide (Ozempic, Wegovy, Wegovy HD, Rybelsus) and orforglipron (Foundayo). Tirzepatide (Mounjaro, Zepbound) is a dual GIP/GLP-1 agonist. Retatrutide and efpeglenatide are not approved and have no brand names.

Is Ozempic the same as Wegovy?

Yes, both contain semaglutide. Ozempic is approved for type 2 diabetes at doses up to 2 mg weekly. Wegovy is approved for obesity at doses up to 2.4 mg weekly. The active ingredient and mechanism are identical; the brand names reflect different FDA indications and dosing schedules.

What is the generic name for Zepbound?

Tirzepatide. Zepbound is the brand name for tirzepatide approved for obesity. Mounjaro is the brand name for the same drug approved for type 2 diabetes. No generic version is available; tirzepatide is under patent protection until at least 2036.

Are compounded semaglutide and Ozempic the same thing?

They contain the same active ingredient (semaglutide) but are not the same product. Ozempic is FDA-approved and manufactured by Novo Nordisk under strict quality controls. Compounded semaglutide is prepared by a compounding pharmacy, is not FDA-approved, and is legal only under specific shortage conditions. They are not interchangeable in pharmacy or insurance systems.

What is the strongest GLP-1 medication?

Among approved products, tirzepatide (Zepbound) has the largest trial weight loss, up to nearly 21% at 72 weeks versus 3% on placebo per GoodRx's April 6, 2026 summary of the SURMOUNT-1 data, followed by Wegovy HD 7.2 mg at about 19% and Wegovy 2.4 mg at about 15%. Retatrutide, a triple agonist, is still investigational and not FDA-approved as of September 4, 2026, so it does not belong in this comparison yet.

Why does semaglutide have three different names?

Semaglutide is marketed under three brand names to distinguish different indications and formulations: Ozempic (injectable for diabetes), Wegovy (injectable for obesity), and Rybelsus (oral for diabetes). The FDA grants separate approvals for separate indications, which allows the manufacturer to use different brand names and pricing.

Can I switch from Ozempic to Wegovy?

Yes, with provider approval. Both contain semaglutide. The switch typically involves adjusting the dose (Ozempic max is 2 mg; Wegovy max is 2.4 mg) and changing the prescription to reflect the obesity indication. Insurance coverage may differ between the two brand names even though the drug is identical.

What is the difference between Mounjaro and Zepbound?

None, except the FDA indication. Both contain tirzepatide at identical doses (2.5 mg to 15 mg). Mounjaro is approved for type 2 diabetes. Zepbound is approved for obesity. The distinction affects insurance coverage and prescribing criteria but not the medication itself.

Are there any oral GLP-1 medications?

Yes, four as of September 4, 2026. Rybelsus (3, 7, 14 mg) and the Ozempic tablet (1.5, 4, 9 mg) are semaglutide for type 2 diabetes; the Wegovy tablet (1.5 to 25 mg) is semaglutide for weight management; and Foundayo (orforglipron, 0.8 to 17.2 mg), approved April 1, 2026, is for obesity. The semaglutide tablets must be taken on an empty stomach with a wait before eating; Foundayo has no food or water restrictions.

When will generic Ozempic be available?

Not before 2034. Semaglutide is under patent protection until 2031 to 2033, depending on the specific patent. Generic manufacturers typically file applications 6 to 12 months before patent expiration, with approval taking another 12 to 18 months. Realistically, generic semaglutide is unlikely before 2034.

What does "compounded tirzepatide" mean?

Compounded tirzepatide is tirzepatide prepared by a compounding pharmacy in response to an individual prescription. It is not FDA-approved. Compounding is legal under Section 503A of the FDCA when the brand-name drug is in shortage or when a patient requires a dose or formulation not commercially available. It uses the generic drug name (tirzepatide) rather than brand names (Mounjaro, Zepbound).

Is Trulicity the same as Ozempic?

No. Trulicity contains dulaglutide; Ozempic contains semaglutide. Both are once-weekly GLP-1 receptor agonists approved for type 2 diabetes, but they are different molecules with different efficacy and side effect profiles. Head-to-head trials show semaglutide produces slightly greater A1C reduction and weight loss than dulaglutide.

What is the newest GLP-1 medication?

Foundayo (orforglipron), approved by the FDA on April 1, 2026 for obesity or overweight with a weight-related condition, is the newest GLP-1 medication and the first small-molecule GLP-1 pill. Retatrutide has not been approved; an earlier version of this answer was wrong on that point.

What is another name for GLP-1?

GLP-1 stands for glucagon-like peptide-1, a gut hormone in the incretin family. The drug class is called GLP-1 receptor agonists (GLP-1 RAs), incretin mimetics or, loosely, incretin therapies. Tirzepatide is a GIP and GLP-1 receptor agonist, sometimes called a dual incretin. Brand names such as Ozempic, Wegovy, Mounjaro, Zepbound and Foundayo are all products within that class, per their prescribing information.

Who should not take a GLP-1 medication?

Every approved product in this class carries the same contraindication: a personal or family history of medullary thyroid carcinoma, or Multiple Endocrine Neoplasia syndrome type 2, plus a prior serious hypersensitivity reaction to the drug (Wegovy label revised 06/2026, Zepbound label revised 08/2026). The labels also advise stopping at least two months before a planned pregnancy and warn against use with other GLP-1-containing products. Your prescriber screens for all of this.

What are the brand names of GLP-1 drugs?

As of September 4, 2026: Byetta and Bydureon BCise (exenatide), Victoza and Saxenda (liraglutide), Adlyxin (lixisenatide), Trulicity (dulaglutide), Ozempic, Rybelsus and Wegovy including Wegovy HD (semaglutide), Mounjaro and Zepbound (tirzepatide) and Foundayo (orforglipron). Tanzeum (albiglutide) was withdrawn in 2018. No other GLP-1 brand exists in the U.S., per FDA's approvals lists.

Sources

  1. Jastreboff AM et al. Tirzepatide Once Weekly for the Treatment of Obesity. New England Journal of Medicine. 2022.
  2. Wilding JPH et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity. New England Journal of Medicine. 2021.
  3. Sattar N et al. Tirzepatide versus semaglutide for weight loss: a meta-analysis of randomized controlled trials. Lancet Diabetes Endocrinology. 2024.
  4. U.S. Food and Drug Administration. Novel Drug Approvals for 2026 (Foundayo, orforglipron, April 1, 2026). https://www.fda.gov/drugs/novel-drug-approvals-fda/novel-drug-approvals-2026
  5. Davies MJ et al. Gastric emptying and glycemic control with tirzepatide versus placebo. Diabetes Care. 2023.
  6. Jall S et al. Glucagon receptor agonism and energy expenditure in humans. Diabetes Care. 2024.
  7. Lingvay I et al. Real-world persistence and outcomes with GLP-1 receptor agonists for obesity. Obesity. 2024.
  8. Wilding JPH et al. Twelve-month persistence with GLP-1 receptor agonists: a systematic review. Diabetes Obesity and Metabolism. 2023.
  9. Nauck MA et al. GLP-1 receptor agonists in the treatment of type 2 diabetes: state-of-the-art. Molecular Metabolism. 2021.
  10. Drucker DJ. Mechanisms of Action and Therapeutic Application of Glucagon-like Peptide-1. Cell Metabolism. 2018.
  11. FDA Drug Shortage Database. Semaglutide and tirzepatide shortage status. Accessed April 2026.
  12. Frias JP et al. Efficacy and safety of dulaglutide versus semaglutide: a systematic review and network meta-analysis. Diabetes Therapy. 2021.
  13. Pi-Sunyer X et al. A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management. New England Journal of Medicine. 2015.
  14. IQVIA National Prescription Audit. GLP-1 receptor agonist prescription trends 2012-2023. 2024.
  15. U.S. Food and Drug Administration. Novel Drug Approvals for 2026, seen September 4, 2026. https://www.fda.gov/drugs/novel-drug-approvals-fda/novel-drug-approvals-2026
  16. Eli Lilly. FDA approves Foundayo (orforglipron), press release with ATTAIN-1 results and dose strengths, April 1, 2026. https://www.prnewswire.com/news-releases/fda-approves-lillys-foundayo-orforglipron-the-only-glp-1-pill-for-weight-loss-that-can-be-taken-any-time-of-day-without-food-or-water-restrictions-302731485.html
  17. Novo Nordisk. Wegovy (semaglutide) injection and tablets prescribing information, revised 06/2026. https://www.novo-pi.com/wegovy.pdf
  18. Eli Lilly. Zepbound (tirzepatide) prescribing information, revised 08/2026. https://pi.lilly.com/us/zepbound-uspi.pdf
  19. Eli Lilly. Mounjaro (tirzepatide) prescribing information, revised 08/2026. https://pi.lilly.com/us/mounjaro-uspi.pdf
  20. Novo Nordisk. Ozempic savings offer and tablet strengths, seen September 4, 2026. https://www.novocare.com/diabetes/products/ozempic/savings-offer.html
  21. Novo Nordisk. What to pay for Wegovy (pen, HD and tablet), seen September 4, 2026. https://www.wegovy.com/obesity/what-to-pay-for-wegovy.html
  22. GoodRx. GLP-1 drugs comparison (trial weight-loss summaries), April 6, 2026. https://www.goodrx.com/classes/glp-1-agonists/glp-1-drugs-comparison
  23. GoodRx. GLP-1 drugs cost and savings (generic liraglutide prices), August 13, 2026. https://www.goodrx.com/classes/glp-1-agonists/glp-1-drugs-cost-and-savings
  24. U.S. FDA. Declaratory order: resolution of the tirzepatide shortage, December 19, 2024. https://www.fda.gov/media/185577/download
  25. U.S. FDA. Declaratory order: resolution of the semaglutide injection shortage, February 21, 2025. https://www.fda.gov/media/185526/download
  26. U.S. FDA. FDA's concerns with unapproved GLP-1 drugs used for weight loss, adverse-event counts as of May 31, 2026. https://www.fda.gov/drugs/postmarket-drug-safety-information-patients-and-providers/fdas-concerns-unapproved-glp-1-drugs-used-weight-loss

Platform Disclaimer. FormBlends is a digital health platform that connects patients with licensed providers and U.S.-based pharmacies. We do not manufacture, prescribe, or dispense medication directly. All clinical decisions are made by independent licensed providers.

Compounded Medication Notice. Compounded semaglutide and tirzepatide are not FDA-approved. They are prepared by a state-licensed compounding pharmacy in response to an individual prescription. Compounded medications have not undergone the same review process as FDA-approved drugs and are not interchangeable with brand-name products.

Results Disclaimer. Individual results vary. Weight-loss outcomes depend on diet, exercise, adherence, baseline weight, and individual response to treatment. Statements about average outcomes reference published clinical trial data, which may differ from real-world results.

Trademark Notice. Ozempic, Wegovy, Rybelsus, Mounjaro, Zepbound, Foundayo, Trulicity, Victoza, Saxenda, Byetta, Bydureon, Adlyxin, and Tanzeum are registered trademarks of their respective owners. FormBlends is not affiliated with, endorsed by, or sponsored by Novo Nordisk, Eli Lilly and Company, GlaxoSmithKline, Sanofi, Boehringer Ingelheim, or any other pharmaceutical manufacturer.

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Original FDA product-record map · August 30, 2026

A GLP-1 list needs seven fields—not just brand names

We organized the class around verifiable product records so sibling brands, combination products, discontinued entries, and multi-receptor drugs remain distinguishable.

Record fieldExampleWhat it prevents
Brand + ingredientOzempic · semaglutideMistaking a brand for a unique molecule
Receptor classGLP-1 only or multi-receptorFlattening different mechanisms into one class label
Route + strengthInjection or tablet; product-specific amountsCross-product dose equivalence
Labeled useExact indication from the current labelTransferring one sibling brand's use to another
Application + statusNDA/BLA and current marketing recordListing discontinued or development products as current

A maintainable GLP-1 list is a product database: brand, ingredient, receptor class, route, strengths, labeled use, application, and current status.

Primary-source check: FDA 2026 GLP-1 product review · Drugs@FDA

Editorial update

What to know before deciding

Updated Aug 30, 2026

GLP-1-related products should be compared as product records, not a flat brand list. Match every brand to its ingredient, receptor targets, route, labeled use, FDA application, and current status.

Map brand to generic ingredient.

Separate GLP-1-only from multi-receptor products.

Include route, label, application, and status.

Questions answered on this page

What drugs are GLP-1 receptor agonists?
The current list includes products built around semaglutide, liraglutide, dulaglutide, exenatide, lixisenatide, tirzepatide, and related combinations.
Which brands share an ingredient?
Ozempic, Wegovy, and oral semaglutide products share semaglutide while remaining separate products.
How should discontinued and current products be shown?
Use current FDA application and marketing-status records beside every entry.

Research Snapshot

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Check the current prescribing information, regulatory status, and trial source before treating an investigational or newly approved medication as interchangeable with an established therapy.
Check before ordering

Regulatory status, labels, trial records, and sponsor updates can change quickly for obesity-drug pipeline pages. This snapshot is designed to make verification easier, not to replace checking the official source before making a medical or purchase decision. Last page review: 2026-08-30.

Evidence standard

How this page was source-checked

Editorial policy

FormBlends does not claim an individual clinician byline unless a named reviewer is available. For this page, the editorial team checks medical and regulatory claims against primary sources, clinical trials, public datasets, and regulator guidance.

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Research sources used to frame this page

For GLP-1 Receptor Agonist Drug Names: The Complete Reference Guide for Every FDA-Approved and Compounded Option, FormBlends checks the page topic against primary trials, systematic reviews, guidelines, and current PubMed-indexed literature where available. These citations are context, not medical advice, proof of eligibility, or a claim that every study applies to every patient.

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These pages separate verified facts, commercial terms, and unresolved claims so you can check the evidence before choosing a provider.

GLP-1 decision path

Use this page to decide if a provider review is the right next step

Direct answer

GLP-1 Receptor Agonist Drug Names: The Complete Reference Guide for Every FDA-Approved and Compounded Option research is most useful when it helps you compare eligibility, expected results, side effects, cost, and the supervision needed before treatment.

Evidence check

The strongest GLP-1 pages connect the practical answer to clinical trials, FDA labeling where applicable, and real access constraints.

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A licensed clinician still needs to review health history, contraindications, current medications, side effects, and dose escalation.

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When the page matches your goal, continue into the FormBlends get-started flow so the intake can route you toward the right prescription review path.

Original tools and data

Use the FormBlends research stack

These assets are built to be useful beyond a single article: shareable data pages, calculators, provider comparisons, and safety checks that give Google and readers something original to crawl.

Editorial refresh

Practical 2026 note for GLP

This update makes GLP more specific by tying semaglutide, tirzepatide, retatrutide, cash-pay pricing, safety signals, glp to the page's original clinical, cost, access, or comparison angle.

The goal is to make the article more useful for people who already know the headline question and need page-level specifics, not another interchangeable glp-1 weight loss summary.

For 2026 review, the content emphasizes current verification, treatment fit, and patient-safety questions that can be discussed with a qualified provider.

GLP custom 2026 image for glp-1 weight loss on FormBlends

Custom 2026 image for GLP, glp-1 weight loss, and better treatment decision-making.

Image description: Unique image for this page covering GLP, glp-1 weight loss, safety, cost, provider selection, and patient decision-making.

Medical Disclaimer: This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication or treatment. FormBlends articles are source-checked against medical and regulatory references, but they are not a substitute for a personal medical consultation.

Written by FormBlends Editorial Research

Prepared by FormBlends Editorial Research. Claims are checked against primary regulatory, trial, label, and public-health sources where available. Reviewed against primary medical, regulatory, and trial sources for accuracy, sourcing, and patient-safety framing.

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