NDC 70882-125
Metformin Hydrochloride 850 mg tablet, film coated
On the label: Cambridge Therapeutics Technologies, LLC. It's repackaged: Cambridge Therapeutics Technologies, LLC rebottles it from Ascend Laboratories, LLC's NDC 67877-218.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it | No problems foundAug 30, 2019 · 6 inspections |
| Alkem Laboratories Limited | Baddi Solan, India | Makes it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
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, film coated
- Strength
- 850 mg
- Approval
- ANDA ANDA091184
- On the market since
- Jan 31, 2011
- Package NDCs
70882-125-30- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?