NDC 70934-792
Metformin Hydrochloride 750 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 Ascend Laboratories, LLC's NDC 67877-414.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Recalls
- Nov 2, 2016 · Class II · Ascend Laboratories LLC
Presence of Foreign Tablets/Capsules; report of Amlodipine Tablets found in 1000 count bottles of Metformin Hydrochloride Tablets USP
Lots: Lot 6121056, exp 5/2019
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Metformin: every company that makes it
- Form
- tablet, extended release
- Strength
- 750 mg
- Approval
- ANDA ANDA206145
- On the market since
- Sep 11, 2020
- Package NDCs
70934-792-30- Official label
- DailyMed (National Library of Medicine), updated Oct 7, 2020
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