Metformin Hydrochloride
- Product NDC
- 13668-012
- 11-digit product format
- 136680012
- Labeler code
- 13668
- Product ID
- 13668-012_03e39e4a-a01e-454c-af1f-d1e5ab30fea1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals L
- Application
- ANDA090014
- Marketing category
- ANDA
- Marketing start
- 2009-12-30
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDRO
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record