Adults with type 2 diabetes, together with diet and exercise, to improve blood sugar.
Sources last read
Brand guide · Tirzepatide
What is Mounjaro?
Mounjaro is a weekly tirzepatide injection for type 2 diabetes in adults and children age 10 and older.
Source for this answer
Source: Current FDA label, checked 2026-08-12
Source: Current FDA label, checked 2026-08-12
Explore Mounjaro
Approved uses
What is Mounjaro approved to treat?
Children age 10 and older with type 2 diabetes, together with diet and exercise.
Adults with type 2 diabetes and established heart or blood vessel disease. This use lowers the risk of heart attack, stroke and heart-related death.
The product itself
Available forms and strengths
Single-dose pen
1 dose
Single-dose vial
1 dose
Multi-dose vial
4 doses
Single-patient-use KwikPen
4 doses
Key product facts
What matters first
- Medicine
- Tirzepatide
- How often
- Once weekly, at any time of day
- Starting dose
- 2.5 mg
- Highest labeled dose
- 15 mg
Eli Lilly and Company makes Mounjaro under NDA 215866. Mounjaro comes as a shot under the skin.
Same medicine, different label
How is Mounjaro different from Zepbound?
Mounjaro and Zepbound both contain tirzepatide. Mounjaro is approved for type 2 diabetes. Zepbound is approved for weight-related care. Their dose plans are not the same.
Read the Zepbound overview- 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