METFORMIN HYDROCHLORIDE
- Product NDC
- 68645-539
- 11-digit product format
- 686450539
- Labeler code
- 68645
- Product ID
- 68645-539_b5703a75-f525-6737-e053-2995a90a0b1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA203686
- Marketing category
- ANDA
- Marketing start
- 2014-12-09
- Marketing end
- 2021-01-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record