NDC 70934-134
Metformin Hydrochloride 500 mg tablet, extended release
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from TAGI Pharma, Inc.'s NDC 51224-007.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| CSPC Ouyi Pharmaceutical Co., Ltd. | Shijiazhuang, China | Makes it, tests it and packages it | Problems found, fixed voluntarilySep 5, 2024 · 8 inspections |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Metformin: every company that makes it
- Form
- tablet, extended release
- Strength
- 500 mg
- Approval
- ANDA ANDA078321
- On the market since
- Jun 6, 2018
- Package NDCs
70934-134-3070934-134-6070934-134-9070934-134-98- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?