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Brand-name prescription medicine

Mounjaro

Generic name: Tirzepatide

FDA application holder: Eli Lilly and Co

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Mounjaro?
Mounjaro is a brand name of Tirzepatide, a prescription medicine. The FDA NDC Directory lists 24 Mounjaro products in 12 strengths and forms.
Who makes Mounjaro?
Eli Lilly and Co holds the FDA application for Mounjaro (NDA215866, approved May 13, 2022). 1 other company (repackagers or distributors) also list Mounjaro products.
Is there a generic or store brand of Mounjaro?
Yes. The FDA NDC Directory lists 30 other products with the same active ingredients, strength and form as a Mounjaro product. Ask your pharmacist whether one is right for you.
What do pharmacies pay for Mounjaro?
CMS lists a National Average Drug Acquisition Cost (NADAC) for 6 Mounjaro strengths and forms (see the table below). That is what pharmacies pay to buy it, not what you pay: your price depends on your insurance and your pharmacy.
Has Mounjaro been recalled?
No recall linked to Mounjaro products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Mounjaro is

Each Mounjaro product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Tirzepatide · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
tirzepatide 10 mg/0.5 mL
injection, solution (subcutaneous)
Mounjaro 2 products, 1 company DailyMed
tirzepatide 12.5 mg/0.5 mL
injection, solution (subcutaneous)
Mounjaro 2 products, 1 company DailyMed
tirzepatide 12.5 mg/mL
injection, solution (subcutaneous)
Mounjaro 3 products, 1 company DailyMed
tirzepatide 15 mg/0.5 mL
injection, solution (subcutaneous)
Mounjaro 2 products, 1 company DailyMed
tirzepatide 16.7 mg/mL
injection, solution (subcutaneous)
Mounjaro 3 products, 1 company DailyMed
tirzepatide 2.5 mg/0.5 mL
injection, solution (subcutaneous)
Mounjaro 2 products, 1 company DailyMed
tirzepatide 20.8 mg/mL
injection, solution (subcutaneous)
Mounjaro 3 products, 1 company DailyMed
tirzepatide 25 mg/mL
injection, solution (subcutaneous)
Mounjaro 3 products, 1 company DailyMed
tirzepatide 4.17 mg/mL
injection, solution (subcutaneous)
Mounjaro 3 products, 1 company DailyMed
tirzepatide 5 mg/0.5 mL
injection, solution (subcutaneous)
Mounjaro 2 products, 1 company DailyMed
tirzepatide 7.5 mg/0.5 mL
injection, solution (subcutaneous)
Mounjaro 2 products, 1 company DailyMed
tirzepatide 8.33 mg/mL
injection, solution (subcutaneous)
Mounjaro 3 products, 1 company DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Tirzepatide →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Mounjaro products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA215866Eli Lilly and CoMay 13, 202224

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Mounjaro, by strength and form
Strength and formGeneric or brandPharmacies pay
tirzepatide 10 mg/0.5 mL
injection, solution
Brand: Mounjaro $538.76 per mL
tirzepatide 12.5 mg/0.5 mL
injection, solution
Brand: Mounjaro $538.59 per mL
tirzepatide 15 mg/0.5 mL
injection, solution
Brand: Mounjaro $538.57 per mL
tirzepatide 2.5 mg/0.5 mL
injection, solution
Brand: Mounjaro $538.75 per mL
tirzepatide 5 mg/0.5 mL
injection, solution
Brand: Mounjaro $538.70 per mL
tirzepatide 7.5 mg/0.5 mL
injection, solution
Brand: Mounjaro $538.74 per mL

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that list Mounjaro

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Mounjaro products.

Recalls

No recall linked to Mounjaro products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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