Glipizide
- Product NDC
- 50090-6996
- 11-digit product format
- 500906996
- Labeler code
- 50090
- Product ID
- 50090-6996_d1e08a73-ecab-4e76-a661-aa41a0747662
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 1995-02-27
- 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 |
|---|
| 50090-6996-0 | 50090699600 | 90 TABLET in 1 BOTTLE (50090-6996-0) | 90 tablet | 2023-12-27 | No | No | Historical |