METFORMIN HYDROCHLORIDE
- Product NDC
- 43063-507
- 11-digit product format
- 430630507
- Labeler code
- 43063
- Product ID
- 43063-507_97cad7a2-7173-a1a7-e053-2a95a90ae6af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077064
- Marketing category
- ANDA
- Marketing start
- 2005-09-28
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record