Metformin Hydrochloride
- Product NDC
- 70518-0034
- 11-digit product format
- 705180034
- Labeler code
- 70518
- Product ID
- 70518-0034_800e63f4-9c22-1d7a-e053-2991aa0af80d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075967
- Marketing category
- ANDA
- Marketing start
- 2016-12-02
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 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