Metformin Hydrochloride
- Product NDC
- 35356-922
- 11-digit product format
- 353560922
- Labeler code
- 35356
- Product ID
- 35356-922_496920c3-e868-4a0d-b52e-f04137c16d5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077095
- Marketing category
- ANDA
- Marketing start
- 2005-01-14
- 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