NDC 70934-207
metformin hydrochloride 1000 mg tablet
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals..
It's a repackaged product (source NDC 23155-104, which isn't on a current label).
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Denton Pharma, Inc. DBA Northwind Pharmaceuticals. uses for other drugs.
Product details
- Generic drug
- Metformin: see every company that makes it
- Form
- tablet
- Strength
- 1000 mg
- Approval
- ANDA ANDA090564
- On the market since
- Dec 11, 2018
- Package NDCs
70934-207-3070934-207-6070934-207-90- Official label
- DailyMed (National Library of Medicine), updated Aug 9, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?