Glipizide
- Product NDC
- 68788-4017
- 11-digit product format
- 687884017
- Labeler code
- 68788
- Product ID
- 68788-4017_4d490a3a-abdc-4ff4-83fb-f302f51e3023
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- 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, 310490 |
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 |
|---|
| 68788-4017-1 | 68788401701 | 100 TABLET in 1 BOTTLE (68788-4017-1) | 100 tablet | 2025-08-29 | No | No | Historical |
| 68788-4017-3 | 68788401703 | 30 TABLET in 1 BOTTLE (68788-4017-3) | 30 tablet | 2025-08-29 | No | No | Historical |
| 68788-4017-6 | 68788401706 | 60 TABLET in 1 BOTTLE (68788-4017-6) | 60 tablet | 2025-08-29 | No | No | Historical |
| 68788-4017-8 | 68788401708 | 18 TABLET in 1 BOTTLE (68788-4017-8) | 18 tablet | 2025-08-29 | No | No | Historical |
| 68788-4017-9 | 68788401709 | 90 TABLET in 1 BOTTLE (68788-4017-9) | 90 tablet | 2025-08-29 | No | No | Historical |