Glipizide
- Product NDC
- 50090-7734
- 11-digit product format
- 500907734
- Labeler code
- 50090
- Product ID
- 50090-7734_017828fd-5bec-452c-8e2e-28d8205e9e80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
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#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7734-0 | 50090773400 | 30 TABLET in 1 BOTTLE (50090-7734-0) | 30 tablet | 2025-10-28 | No | No | Current |
| 50090-7734-1 | 50090773401 | 60 TABLET in 1 BOTTLE (50090-7734-1) | 60 tablet | 2025-10-28 | No | No | Current |
| 50090-7734-2 | 50090773402 | 100 TABLET in 1 BOTTLE (50090-7734-2) | 100 tablet | 2025-10-28 | No | No | Current |
| 50090-7734-5 | 50090773405 | 90 TABLET in 1 BOTTLE (50090-7734-5) | 90 tablet | 2025-10-28 | No | No | Current |
| 50090-7734-6 | 50090773406 | 180 TABLET in 1 BOTTLE (50090-7734-6) | 180 tablet | 2025-10-28 | No | No | Current |