Glipizide
- Product NDC
- 50090-7735
- 11-digit product format
- 500907735
- Labeler code
- 50090
- Product ID
- 50090-7735_6d8b63b5-34ba-47ec-aadc-80d0cc8e0dee
- 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7735-0 | 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 |
|---|
| 50090-7735-0 | 50090773500 | 90 TABLET in 1 BOTTLE (50090-7735-0) | 90 tablet | 2025-10-28 | No | No | Historical |