Metformin Hydrochloride
- Product NDC
- 71335-0592
- 11-digit product format
- 713350592
- Labeler code
- 71335
- Product ID
- 71335-0592_e96e7cbc-1c4b-4ef2-87dc-35a1826e5c0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075967
- Marketing category
- ANDA
- Marketing start
- 2002-01-29
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record