Metformin Hydrochloride
- Product NDC
- 50436-0248
- 11-digit product format
- 504360248
- Labeler code
- 50436
- Product ID
- 50436-0248_d1d78349-7612-4471-aa7c-b57372bf050e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA076706
- Marketing category
- ANDA
- Marketing start
- 2004-12-16
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 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