Metformin Hydrochloride
- Product NDC
- 70518-0973
- 11-digit product format
- 705180973
- Labeler code
- 70518
- Product ID
- 70518-0973_8e646f05-1c38-582c-e053-2995a90a3157
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203755
- Marketing category
- ANDA
- Marketing start
- 2018-01-22
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record