Glipizide
- Product NDC
- 49999-108
- 11-digit product format
- 499990108
- Labeler code
- 49999
- Product ID
- 49999-108_4eda2774-ce9d-44cc-9a89-e200c89efab4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA074305
- Marketing category
- ANDA
- Marketing start
- 1995-04-07
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record