Glipizide
- Product NDC
- 50436-6462
- 11-digit product format
- 504366462
- Labeler code
- 50436
- Product ID
- 50436-6462_d16ad8b3-059d-41bd-8942-0e5ee0ab3a1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 1995-02-27
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 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