Glipizide and Metformin Hydrochloride
- Product NDC
- 0179-0205
- 11-digit product format
- 001790205
- Labeler code
- 0179
- Product ID
- 0179-0205_7bc0b29f-7757-d02f-e053-2991aa0a117f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide and Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA077270
- Marketing category
- ANDA
- Marketing start
- 2016-04-22
- Marketing end
- 2020-01-31
- Substance
- GLIPIZIDE; METFORMIN HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record