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Brand-name prescription medicine

TOUJEO Max

Generic name: Insulin glargine

FDA application holder: Sanofi US Services

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 TOUJEO Max?
TOUJEO Max is a brand name of Insulin glargine, a prescription medicine. The FDA NDC Directory lists 2 TOUJEO Max products in 1 strength and form.
Who makes TOUJEO Max?
Sanofi US Services holds the FDA application for TOUJEO Max (BLA206538, approved February 25, 2015). 1 other company (repackagers or distributors) also list TOUJEO Max products.
Is there a generic or store brand of TOUJEO Max?
Yes. The FDA NDC Directory lists 4 other products with the same active ingredients, strength and form as a TOUJEO Max product. Ask your pharmacist whether one is right for you.
What do pharmacies pay for TOUJEO Max?
CMS lists a National Average Drug Acquisition Cost (NADAC) for 1 TOUJEO Max strength and form (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 TOUJEO Max been recalled?
No recall linked to TOUJEO Max products (by their NDC code or label) appears in the FDA enforcement reports we use.

What TOUJEO Max is

Each TOUJEO Max 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.

Insulin glargine · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
insulin glargine 300 units/mL
injection, solution (subcutaneous)
TOUJEO Max 4 products, 2 companies DailyMed

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

FDA approval

  • BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
FDA applications of TOUJEO Max products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
BLA206538Sanofi US ServicesFebruary 25, 20152

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 TOUJEO Max, by strength and form
Strength and formGeneric or brandPharmacies pay
insulin glargine 300 units/mL
injection, solution
Brand: TOUJEO Max $91.28 per mL
Generic of the same strength and form: $26.96–$26.99 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 TOUJEO Max

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

Recalls

No recall linked to TOUJEO Max 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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