Glipizide
- Product NDC
- 71335-2540
- 11-digit product format
- 713352540
- Labeler code
- 71335
- Product ID
- 71335-2540_f0974f5e-83f9-4296-bf0d-535f2edfaa08
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA214874
- Marketing category
- ANDA
- Marketing start
- 2023-10-03
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X7WDT95N5C | GLIPIZIDE | 29094-61-9 | GLIPIZIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2540-1 | 71335254001 | 60 TABLET in 1 BOTTLE (71335-2540-1) | 60 tablet | 2024-12-10 | No | No | Historical |
| 71335-2540-2 | 71335254002 | 30 TABLET in 1 BOTTLE (71335-2540-2) | 30 tablet | 2024-12-10 | No | No | Historical |
| 71335-2540-3 | 71335254003 | 100 TABLET in 1 BOTTLE (71335-2540-3) | 100 tablet | 2024-12-10 | No | No | Historical |
| 71335-2540-4 | 71335254004 | 120 TABLET in 1 BOTTLE (71335-2540-4) | 120 tablet | 2024-12-10 | No | No | Historical |
| 71335-2540-5 | 71335254005 | 90 TABLET in 1 BOTTLE (71335-2540-5) | 90 tablet | 2024-12-10 | No | No | Historical |
| 71335-2540-6 | 71335254006 | 20 TABLET in 1 BOTTLE (71335-2540-6) | 20 tablet | 2024-12-10 | No | No | Historical |
| 71335-2540-7 | 71335254007 | 180 TABLET in 1 BOTTLE (71335-2540-7) | 180 tablet | 2024-12-10 | No | No | Historical |