Glipizide and Metformin Hydrochloride
- Product NDC
- 50436-0874
- 11-digit product format
- 504360874
- Labeler code
- 50436
- Product ID
- 50436-0874_abe3c6cc-1c57-448d-83b9-42faf3efa58d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077270
- Marketing category
- ANDA
- Marketing start
- 2005-10-28
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 3 mg/1; mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record