METFORMIN HYDROCHLORIDE
- Product NDC
- 70518-0408
- 11-digit product format
- 705180408
- Labeler code
- 70518
- Product ID
- 70518-0408_848d363a-523a-1fc3-e053-2a91aa0af740
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201991
- Marketing category
- ANDA
- Marketing start
- 2017-04-06
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record