Quick answers
- What is Glumetza?
- Glumetza is a brand name of Metformin hydrochloride, a prescription medicine. The FDA NDC Directory lists 3 Glumetza products in 2 strengths and forms.
- Who makes Glumetza?
- Santarus Inc holds the FDA application for Glumetza (NDA021748, approved June 3, 2005).
- Is there a generic or store brand of Glumetza?
- Yes. The FDA NDC Directory lists 21 other products with the same active ingredients, strength and form as a Glumetza product, 21 of them generic. Ask your pharmacist whether one is right for you.
- Has Glumetza been recalled?
- No recall linked to Glumetza products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Glumetza is
Each Glumetza 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.
Metformin hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| metformin hydrochloride 1000 mg tablet, film coated, extended release (oral) | Glumetza | 11 products, 10 companies | — |
| metformin hydrochloride 500 mg tablet, film coated, extended release (oral) | Glumetza | 10 products, 9 companies | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Metformin hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021748 | Santarus Inc | June 3, 2005 | 3 |
Companies that list Glumetza
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Glumetza products.
- Santarus, Inc.3 products
Recalls
No recall linked to Glumetza products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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.