METFORMIN HYDROCHLORIDE
- Product NDC
- 50090-1981
- 11-digit product format
- 500901981
- Labeler code
- 50090
- Product ID
- 50090-1981_749df52d-96fc-4f94-a029-e9d27a2f6d2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077336
- Marketing category
- ANDA
- Marketing start
- 2006-02-09
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record