Adults with type 2 diabetes, together with diet and exercise, to improve blood sugar.
Sources last read
Brand guide · Semaglutide
What is Ozempic?
Ozempic is a brand of Semaglutide. FDA has approved it for 3 uses. People take it once weekly, on the same day each week, at any time of day, with or without meals. The first labeled dose is 0.25 mg. The highest is 2 mg.
Source: Current FDA label, checked 2026-08-12
What matters first
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Approved uses
What is Ozempic approved to treat?
Adults with type 2 diabetes and heart risk, to lower the risk of heart attack, stroke and heart-related death.
Adults with type 2 diabetes and chronic kidney disease, to lower the risk of kidney failure and heart-related death.
The product itself
How Ozempic comes
Single-patient-use pen, 2 mg per 3 mL
4 doses
Single-patient-use pen, 4 mg per 3 mL
4 doses
Single-patient-use pen, 8 mg per 3 mL
4 doses
Single-dose prefilled syringe
1 dose
Novo Nordisk makes Ozempic under NDA 209637. The label says it is given as a shot under the skin.
Same medicine, different label
How is Ozempic different from Wegovy?
Two brand names use this drug. Ozempic is the one for type 2 diabetes. Wegovy is the one for weight-related care. Their dose plans are not the same.
Read the Wegovy overview- Ozempic (semaglutide) injection — FDA-approved Prescribing Information (DailyMed)retrieved 2026-08-12FDA label
- Drugs@FDA approval history — NDA 209637, Ozempic (semaglutide) injectionretrieved 2026-08-12FDA label
- FDA approval letter, NDA 209637 — Ozempic (semaglutide) injection, glycemic control in adults with type 2 diabetesretrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 209637/S-003 — Ozempic cardiovascular event risk reduction in type 2 diabetes with established cardiovascular disease (SUSTAIN 6)retrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 209637/S-025 — Ozempic for reducing sustained eGFR decline, end-stage kidney disease and cardiovascular death in type 2 diabetes with chronic kidney diseaseretrieved 2026-08-12FDA label
- FDA supplement approval letter, NDA 209637/S-009 — addition of a third Ozempic maintenance dose, 2 mg once weeklyretrieved 2026-08-12FDA label