Metformin Hydrochloride
- Product NDC
- 13668-001
- 11-digit product format
- 136680001
- Labeler code
- 13668
- Product ID
- 13668-001_75e262e6-6336-4e6a-b6e3-1fa41337628c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals L
- Application
- ANDA077711
- Marketing category
- ANDA
- Marketing start
- 2007-01-24
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDRO
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record