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Wegovy vs Mounjaro
Wegovy and Mounjaro contain different drugs. Wegovy has a weight-management use; Mounjaro treats type 2 diabetes. Both also have heart-risk uses, with different patient groups covered.
Source for this answer
Source: Read from both FDA labels on DailyMed
Source: Read from both FDA labels on DailyMed
Medically reviewed by Jennifer Montecillo, MD · non-practicing medical reviewerReviewed 2026-08-13every number here is sourced
Wegovy and Mounjaro, line by line
Compare 14 details from the two labels. Side-effect figures from separate trials do not establish which medicine is safer.
| Question | Wegovy | Mounjaro |
|---|---|---|
| What is in it | Semaglutide, which acts on one gut hormone receptor, GLP-1 | Tirzepatide, which acts on two, GIP and GLP-1 |
| Who makes it | Novo Nordisk | Eli Lilly and Company |
| Approved uses | Weight management in eligible adults and adolescents aged 12 and older; heart-risk reduction and certain MASH liver disease in eligible adults | Blood sugar control in type 2 diabetes; heart-risk reduction in adults with type 2 diabetes at high risk |
| Is it approved for weight | Yes | No |
| Is it approved for blood sugar in type 2 diabetes | No | Yes |
| How oftenSame on both labels | Once a week | Once a week |
| When it was approved | 2021-06-04, under NDA 215256 | 2022-05-13, under NDA 215866 |
| Starting dose | 0.25 mg once a week | 2.5 mg once a week; increase only if more blood sugar control is needed, after at least 4 weeks |
| Highest dose | 2.4 mg, or 7.2 mg for weight reduction in adults | 15 mg a week for adults, 10 mg from age 10 |
| Maintenance doses | 1.7, 2.4 or 7.2 mg | No separate maintenance-dose list; further increases depend on blood sugar control |
| How a missed week is handled | Take it if the next dose is more than 2 days off, otherwise skip | Take within 4 days of the missed dose; otherwise skip it |
| Youngest patient covered | Age 12 | Age 10, added in December 2025 |
| Is there a pill | Yes, a tablet at 1.5, 4, 9 and 25 mg, under a separate application | No. Injection only |
| What the label reports for nausea | 44 in 100 at 2.4 mg, against 16 on placebo | 12, 15 and 18 in 100 at 5, 10 and 15 mg, against 4 on placebo |
Product comparison at a glance
- Wegovy
- Semaglutide
- Mounjaro
- Tirzepatide
- Label differences
- 13 of 14 comparison rows differ
- Direct trial
- None published
Has anyone tested Wegovy against Mounjaro directly?
No. Two trials have compared the two ingredients, and each of them lines up with one of these products and not the other.
SURMOUNT-5 ran 72 weeks in 751 adults with obesity and without type 2 diabetes. Its semaglutide arm reached 1.7 mg or 2.4 mg, which is Wegovy’s own maintenance range, and its tirzepatide arm reached 10 mg or 15 mg, which is inside Mounjaro’s range too. But the people in it were being treated for obesity — Wegovy’s approved use, and not one the Mounjaro label carries.
SURPASS-2 ran 40 weeks in 1,879 adults with type 2 diabetes, which is Mounjaro’s use. Its semaglutide arm was 1 mg. That is below Wegovy’s listed maintenance doses, so it does not compare Wegovy at a maintenance dose.
So the trials bracket this pair without landing on it: right population and the wrong semaglutide dose, or right semaglutide dose and the wrong population.
Different approved uses do not prevent researchers from comparing two drugs. They do limit what can be concluded from trials conducted for those uses.
5Comparison details
Which comparison matches the condition being treated?
Wegovy is approved for weight and Mounjaro is approved for blood sugar. If somebody is being treated for weight, Mounjaro is not the label-covered option; if for type 2 diabetes, Wegovy is not.
What makes that easy to miss is that each has a twin under a different name. Mounjaro’s twin is Zepbound: the same tirzepatide, the same maker, the same devices, the same 2.5 mg steps, and a label that covers weight. Wegovy’s twin is Ozempic: the same semaglutide, the same maker, and a label that covers type 2 diabetes.
So the comparison that answers a weight question is Wegovy against Zepbound, and the one that answers a diabetes question is Ozempic against Mounjaro. Those trials match the approved uses and studied doses more closely. They do not establish a direct result for this pair.
Why an off-label prescription needs its own discussion
Use for a condition outside the approved label is called off-label use. The comparisons here describe approved uses; they do not decide whether an off-label prescription suits someone.
What the labels do settle is what happens around it. An approved use brings a printed dose schedule for that use, a reaction table drawn from trials in those patients, and an age range. Mounjaro’s reaction table comes from diabetes trials in people mostly already on other diabetes medicines. Wegovy’s comes from weight trials carried to 2.4 mg.
The nausea figures — 44 in 100 against 12 to 18 in 100 — come from different trial groups. They cannot establish a difference in nausea risk between the two medicines.
Only one of the two has a tablet, and only one has an age-10 approval
Wegovy also exists as a tablet, at 1.5, 4, 9 and 25 mg, under a separate application. Mounjaro is injection only.
Mounjaro reaches further down in age: from 10 years old, added in December 2025, with the ceiling set at 10 mg rather than 15 for those patients. Wegovy covers age 12 and up.
These approvals belong to the named product and dosage form. They do not automatically extend to another product containing the same ingredient.
What about “Mounjaro vs Wegovy”?
Reversing the names does not change the product details or trial results.
Read each result with its own dose, study group and limits, whichever name comes first.
The full label for each
Choose a product below to see its full dose schedule, side effects and storage rules.
Wegovy
Mounjaro
- Wegovy (semaglutide) injection and tablets — FDA-approved Prescribing Information (DailyMed)retrieved 2026-08-12FDA label
- Wegovy (semaglutide) Prescribing Information, revised 06/2026 — Drugs@FDA NDA 215256/S-025retrieved 2026-08-12FDA label
- FDA approval letter, NDA 215256 — Wegovy (semaglutide) injection, chronic weight management in adultsretrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 215256/S-005 — Wegovy in pediatric patients aged 12 years and olderretrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 215256/S-011 — Wegovy cardiovascular risk reduction indication (SELECT)retrieved 2026-08-12FDA label
- FDA accelerated approval letter, NDA 215256/S-024 — Wegovy for noncirrhotic MASH with stage F2 to F3 fibrosisretrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 215256/S-029 — Wegovy injection 7.2 mg once-weekly doseretrieved 2026-08-12FDA label
- FDA approval letter, NDA 218316 — Wegovy (semaglutide) tablets, oral dosage formretrieved 2026-08-12FDA label
- Mounjaro (tirzepatide) injection — FDA-approved Prescribing Information (DailyMed)retrieved 2026-09-13FDA label
- Drugs@FDA approval history — NDA 215866, Mounjaro (tirzepatide) injectionretrieved 2026-08-12FDA label
- FDA approval letter, NDA 215866 — Mounjaro (tirzepatide) injection, glycemic control in adults with type 2 diabetesretrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 215866/S-039 — expansion of the Mounjaro type 2 diabetes indication to pediatric patients aged 10 years and older (trial I8F-MC-GPGV)retrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 215866/S-044 and S-045 — Mounjaro heart-risk reduction and 2.5 mg for ongoing blood sugar controlretrieved 2026-09-13FDA label
- Aronne LJ et al. Tirzepatide as Compared with Semaglutide for the Treatment of Obesity (SURMOUNT-5). N Engl J Med 2025;393(1):26-36 — PubMed 40353578retrieved 2026-08-12Human trial
- SURMOUNT-5 trial registry record — ClinicalTrials.gov NCT05822830retrieved 2026-08-12Human trial
- Frías JP et al. Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes (SURPASS-2). N Engl J Med 2021;385(6):503-515 — PubMed 34170647retrieved 2026-08-12Human trial
- SURPASS-2 trial registry record — ClinicalTrials.gov NCT03987919retrieved 2026-08-12Human trial