Metformin Hydrochloride
- Product NDC
- 42708-075
- 11-digit product format
- 427080075
- Labeler code
- 42708
- Product ID
- 42708-075_883db3c8-1fe1-4f3e-a55a-3e79e3e3ac5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA076269
- Marketing category
- ANDA
- Marketing start
- 2004-06-18
- 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