Glipizide
- Product NDC
- 82804-174
- 11-digit product format
- 828040174
- Labeler code
- 82804
- Product ID
- 82804-174_abe14fb1-e2fa-4c89-8007-fa4c18fd70a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA214874
- Marketing category
- ANDA
- Marketing start
- 2023-10-03
- Substance
- GLIPIZIDE
- Active strength
- 5 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 |
|---|
| 82804-174-30 | 82804017430 | 30 TABLET in 1 BOTTLE (82804-174-30) | 30 tablet | 2024-12-12 | No | No | Historical |
| 82804-174-90 | 82804017490 | 90 TABLET in 1 BOTTLE (82804-174-90) | 90 tablet | 2025-01-20 | No | No | Historical |