Zepbound® vs Mounjaro®: A Simple Breakdown
Learn how Zepbound® and Mounjaro® differ in indications, dosing, and risks, so you can talk with your clinician about what may fit your goals.
- Same active ingredient, different FDA approvals: Zepbound® vs Mounjaro® (FDA-approved for weight management vs FDA-approved for type 2 diabetes).
- Strong clinical results in trials: At higher doses, tirzepatide showed ~20% average weight loss over ~72 weeks in adults with obesity/overweight when combined with diet and activity. Individual results vary. The formulation used in the referenced study is what was later approved and marketed under the brand name Zepbound® for chronic weight management.
- Costs matter: List prices may exceed $1,000/month before insurance; savings programs and coverage may change out-of-pocket costs.
- Dual-action mechanism: Tirzepatide targets both GIP and GLP-1 receptors.
- Safety monitoring required: Boxed warning for thyroid C-cell tumors; GI side effects are common; ongoing clinical follow-up is important.
- Coverage varies by indication: Plans may limit coverage for weight-loss drugs (Zepbound®), while Mounjaro® is generally covered for treating type 2 diabetes.
Disclaimer: Educational content and not medical advice. Discuss any medication with your licensed healthcare provider. Eden coordinates care; licensed providers evaluate and prescribe, and partner pharmacies dispense and label. For FDA-approved drugs, see each manufacturer’s full prescribing information.
About 70% of U.S. adults are overweight or obese (estimates vary by survey period). Interest in Mounjaro® vs Zepbound® is rising. In obesity trials, tirzepatide medication produced ~21% average weight loss over 72 weeks with diet and physical activity (using a formulation later approved as Zepbound®). We’ll cover trial details later.
Both medicines contain tirzepatide but have different FDA approvals: Zepbound® for chronic weight management in eligible adults and Mounjaro® for the treatment of type 2 diabetes. Tirzepatide acts on GLP-1 and GIP receptors, a dual mechanism that helps explain observed weight and glycemic effects when used as labeled.
How They’re Approved (FDA-Labeled Uses)
The FDA identifies a significant difference between Zepbound® and Mounjaro®, despite both containing the same active ingredient. Labels guide how clinicians prescribe or consider off-label use.
Zepbound®: Chronic Weight Management Indication
The FDA approved Zepbound® in November 2023 specifically to manage chronic weight issues. Adults may be eligible if they have:
- A body mass index (BMI) of 30 kg/m² or greater (obesity), or
- A BMI of 27 kg/m² or greater (overweight) with at least one weight-related medical condition
Doctors may prescribe Zepbound® with a reduced-calorie diet and suggest increased physical activity. The SURMOUNT-1 clinical trial showed clinically significant weight reduction compared to placebo (the study formulation became Zepbound®).
Mounjaro®: Type 2 Diabetes Indication
The FDA approved Mounjaro® in May 2022 to improve blood glucose control in adults with type 2 diabetes. Clinical trials showed that Mounjaro® lowered A1C levels effectively when patients combined it with diet and exercise.
Note on off-label use: Because Mounjaro® and Zepbound® contain tirzepatide, clinicians may consider Mounjaro® off-label for weight management in some cases. Only a licensed prescriber can determine whether off-label use is appropriate for an individual patient.
What this means in real life:
- Coverage may follow labeled use.
- Each product comes with different patient information.
- Dosing titration schedules may be similar, but your prescriber may follow the label that matches your condition and product.
While both contain tirzepatide, the key difference is their FDA-approved indications. Your clinician will recommend the option (when clinically appropriate) that fits your diagnosis, goals, coverage, and safety considerations.
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What’s Inside & How They Work
Same active ingredient but different FDA-approved uses
Zepbound® and Mounjaro® both contain tirzepatide. Tirzepatide is a dual GIP/GLP-1 receptor agonist that:
- GLP-1 receptors: slow gastric emptying, boost insulin secretion, and reduce appetite.
- GIP receptors: enhance insulin response and may further influence appetite regulation.
Why labels matter in practice
- Dosing protocols and patient education differ by indication.
- Monitoring needs can differ depending on whether the goal is diabetes management or weight management.
Delivery form and administration overview
Both are once-weekly subcutaneous injections in prefilled pens (abdomen, thigh, or upper arm).
Example dosing (for illustration purposes only; your prescriber determines each plan if clinically appropriate):
- Start: 2.5 mg once weekly for ~4 weeks
- Gradual increases: About every 4 weeks
- Maximum dose: Up to 15 mg weekly, per product labeling
Administration tips (although not a substitute for clinical training): Inject on the same day each week, rotate sites (abdomen, thigh, or upper arm), and confirm the solution is clear and colorless.
What the Research Shows
Weight Management (SURMOUNT trials*):
- What they measured: Change in body weight over ~72 weeks
- What they found: At higher doses, alongside diet and physical activity, participants taking tirzepatide medication lost ~20% on average; many achieved ≥ 5%, and some reached ≥ 20%. Individual results vary.
Type 2 Diabetes (SURPASS trials*):
- What they measured:
- A1C - a lab test that reflects your average blood sugar over ~3 months
- How many people reached A1C < 7%
- What they found: Tirzepatide lowered A1C by up to ~2.4 percentage points (dose-dependent), and more people hit the target compared with study control groups. Weight also tended to go down, though these studies focused on blood sugar first.
*In SURPASS-2 (type 2 diabetes), tirzepatide (5, 10, 15 mg; brand Mounjaro®) was compared with semaglutide 1 mg (brand Ozempic® for type 2 diabetes). Wegovy® 2.4 mg was not evaluated in SURPASS-2. In SURMOUNT-1 (obesity), tirzepatide was compared with a placebo.
Why it matters:
- Trials were designed to answer different questions: weight (Zepbound®) vs blood sugar (Mounjaro®).
- Your clinician will match treatment (when clinically appropriate) to your diagnosis, goals, safety profile, and insurance coverage.
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What the Numbers Mean (And What They Don't)
Clinical trial averages are helpful, but real-world results vary. Factors like how closely you follow the plan, the dose you reach and maintain, your individual response, and coverage/costs can all change outcomes. Your clinician will help interpret the data in the context of your individual health profile.
Safety and Monitoring
Both products contain tirzepatide and carry an FDA boxed warning (applicable to both Zepbound® and Mounjaro®) about thyroid C-cell tumors (seen in animals; it is unknown if this risk occurs in humans). Seek care for neck lumps, hoarseness, trouble swallowing, or shortness of breath.
Common GI effects: nausea, diarrhea, vomiting, constipation (may be dose-dependent and may improve over time, but not guaranteed).
Do not use if you have a personal/family history of MTC, MEN 2, or a known hypersensitivity to tirzepatide. Not recommended during pregnancy; Mounjaro® isn’t for type 1 diabetes. Get urgent help for severe abdominal pain (possible pancreatitis), gallbladder symptoms, persistent vomiting/dehydration, or allergic reactions. Tell your clinician about all medicines and procedures (including anesthesia).
Coverage & Cost
Coverage typically follows the indication:
- Zepbound® (weight management): Often excluded or tightly managed (BMI thresholds, documented lifestyle efforts, weight-related conditions).
- Mounjaro® (type 2 diabetes): More commonly covered for diabetes with diagnosis, recent A1C, and step therapy.
- List price for either can exceed $1,000/month before insurance; savings programs may lower costs for eligible commercial plans.
Conclusion
Zepbound® and Mounjaro® share the same active ingredient but serve different FDA-approved uses, weight management vs type 2 diabetes. The appropriate choice (if any) depends on your diagnosis, goals, safety profile, and coverage. Talk with your clinician about which option (if clinically appropriate) fits your plan and how to monitor progress over time.
Eden is an independent company and is not affiliated with, sponsored by, or endorsed by Eli Lilly and Company or Novo Nordisk; all trademarks are the property of their respective owners.. Names are used here for identification and educational purposes only.
Disclaimer: The FDA does not approve compounded medications for safety, quality, or manufacturing. Prescriptions and a medical evaluation are required for certain products. The information provided on this blog is for general informational purposes only. It is not intended as a substitute for professional advice from a qualified healthcare professional and should not be relied upon as personal health advice. The information contained in this blog is not meant to diagnose, treat, cure, or prevent any disease. Readers are advised to consult with a qualified healthcare professional for any medical concerns, including side effects. Use of this blog's information is at your own risk. The blog owner is not responsible for any adverse effects or consequences resulting from the use of any suggestions or information provided in this blog.
Eden is not a medical provider. Eden connects individuals with independent licensed healthcare providers who independently evaluate each patient to determine whether a prescription treatment program is appropriate. All prescriptions are written at the sole discretion of the licensed provider. Medications are filled by state-licensed pharmacies. Please consult a licensed healthcare provider before making any medical decisions.
Frequently asked questions
They share the same active ingredient, but effectiveness depends on your condition, dose, and individual factors. Labels/uses differ; your clinician will choose what fits your diagnosis and goals (when clinically appropriate).
List prices often >$1,000/month before insurance for a month’s dose. Actual out-of-pocket varies by plan and any savings programs. LillyDirect self-pay vials: $349 (2.5 mg starter) and $499+ for higher doses, per program terms. Manufacturer savings may reduce costs for eligible commercially insured patients; government programs excluded.
Mostly GI (nausea, diarrhea, vomiting, constipation). Many improve over time or with slower titration; ask your clinician.
In obesity trials, tirzepatide produced ~20% average loss over ~72 weeks with diet/activity. Individual results vary.
Anyone with MTC/MEN 2 or tirzepatide hypersensitivity; not recommended in pregnancy. Mounjaro® isn’t for type 1 diabetes.
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References
Aetna. (2024). Zepbound prior authorization with limit policy (6192-C). https://www.aetna.com/products/rxnonmedicare/data/2024/Zepbound_PA_with_Limit_6192-C_P08-2024_R.html
Centers for Disease Control and Prevention, National Center for Health Statistics. (2024). Obesity and severe obesity prevalence in adults: United States, August 2021–August 2023 (NCHS Data Brief No. 508). https://www.cdc.gov/nchs/products/databriefs/db508.htm
Dahl, D., Onishi, Y., Norwood, P., Huh, R., Bray, R., Patel, H., & Rodríguez, Á. (2022). Effect of subcutaneous tirzepatide vs placebo added to titrated insulin glargine on glycemic control in patients with type 2 diabetes: The SURPASS-5 randomized clinical trial. JAMA, 327(6), 534–545. https://doi.org/10.1001/jama.2022.0078
Eli Lilly and Company. (2022). MOUNJARO (tirzepatide) injection, for subcutaneous use: Prescribing information. U.S. Food and Drug Administration. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/215866s000lbl.pdf
Eli Lilly and Company. (2024). ZEPBOUND (tirzepatide) injection, for subcutaneous use: Prescribing information. U.S. Food and Drug Administration. https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/217806s003lbl.pdf
Frías, J. P., Davies, M. J., Rosenstock, J., Pérez Manghi, F. C., Fernández Landó, L., Bergman, B. K., Liu, B., & Fernández, L. (2021). Tirzepatide versus semaglutide once weekly in patients with type 2 diabetes. The New England Journal of Medicine, 385(6), 503–515. https://doi.org/10.1056/NEJMoa2107519
Gasoyan, H., et al. (2025). Changes in weight and glycemic control following obesity pharmacotherapy with semaglutide or tirzepatide in real-world practice. Obesity. https://doi.org/10.1002/oby.24331
Jastreboff, A. M., Aronne, L. J., Ahmad, N. N., Wharton, S., Connery, L., Alves, B., Kiyosue, A., Zhang, S., Liu, B., Bunck, M. C., & Stefanski, A. (2022). Tirzepatide once weekly for the treatment of obesity. The New England Journal of Medicine, 387(3), 205–216. https://doi.org/10.1056/NEJMoa2206038
Office of the Assistant Secretary for Planning and Evaluation (ASPE). (2024). Medicare coverage of anti-obesity medications (Issue Brief). U.S. Department of Health & Human Services. https://aspe.hhs.gov/sites/default/files/documents/127bd5b3347b34be31ac5c6b5ed30e6a/medicare-coverage-anti-obesity-meds.pdf
U.S. Congressional Research Service. (2024). Medicare coverage of GLP-1 drugs (In Focus IF12758). https://www.congress.gov/crs-product/IF12758
Eli Lilly and Company. (2025). Zepbound prior authorization resource guide (payer reference). https://zepbound.lilly.com/assets/pdf/zepbound_Prior_Authorization_Resource_Guide.pdf
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