Glipizide
- Product NDC
- 80425-0549
- 11-digit product format
- 804250549
- Labeler code
- 80425
- Product ID
- 80425-0549_3d87c932-9653-482e-e063-6294a90a3b84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advanced Rx of Tennessee, LLC
- Application
- ANDA214874
- Marketing category
- ANDA
- Marketing start
- 2025-08-29
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glipizide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLIPIZIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X7WDT95N5C |
| Rxcui | 310488 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80425-0549-1 | Glipizide | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 80425-0549-2 | Glipizide | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 80425-0549-3 | Glipizide | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0549-1 | 80425054901 | 30 TABLET in 1 BOTTLE (80425-0549-1) | 30 tablet | 2025-08-29 | No | No | Historical |
| 80425-0549-2 | 80425054902 | 60 TABLET in 1 BOTTLE (80425-0549-2) | 60 tablet | 2025-08-29 | No | No | Historical |
| 80425-0549-3 | 80425054903 | 90 TABLET in 1 BOTTLE (80425-0549-3) | 90 tablet | 2025-08-29 | No | No | Historical |