NDC 66116-370
Metformin Hydrochloride 1000 mg tablet, film coated
On the label: MedVantx, Inc.. It's repackaged from NDC 0093-7214, made by Teva Pharmaceuticals USA, Inc. (Metformin Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants MedVantx, Inc. names for other drugs.
Product details
- Generic drug
- Metformin: every company that makes it
- Form
- tablet, film coated
- Strength
- 1000 mg
- Approval
- ANDA ANDA075978
- On the market since
- Jul 27, 2010
- Package NDCs
66116-370-30- Official label
- DailyMed (National Library of Medicine), updated Jul 27, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?