NDC 72789-105
Metformin hydrochloride 500 mg tablet, extended release
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 76385-128.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Beximco Pharmaceuticals PLC | Tongi, Bangladesh | Makes it | Problems found, fixed voluntarilyMar 30, 2023 · 2 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Recalls
- Aug 19, 2020 · Class II · Bayshore Pharmaceuticals
CGMP Deviations
Lots: Lot #18641; Exp. 05/2021 - Aug 19, 2020 · Class II · Bayshore Pharmaceuticals
CGMP Deviations
Lots: Lot #18657, Exp. 05/2021
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, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA207427
- On the market since
- Jul 17, 2018
- Package NDCs
72789-105-0172789-105-6072789-105-8272789-105-9072789-105-9372789-105-95- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?