Glipizide
- Product NDC
- 50090-7404
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074497
- Marketing category
- ANDA
- Substance
- GLIPIZIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7404-0 | 30 TABLET in 1 BOTTLE (50090-7404-0) | 2024-10-24 | | No | Historical |
| 50090-7404-1 | 60 TABLET in 1 BOTTLE (50090-7404-1) | 2024-10-24 | | No | Historical |
| 50090-7404-2 | 100 TABLET in 1 BOTTLE (50090-7404-2) | 2024-10-24 | | No | Historical |
| 50090-7404-5 | 90 TABLET in 1 BOTTLE (50090-7404-5) | 2024-10-24 | | No | Historical |
| 50090-7404-6 | 180 TABLET in 1 BOTTLE (50090-7404-6) | 2024-10-24 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Glipizide Tablets USP | A-S Medication Solutions | 2024-10-25 | HUMAN PRESCRIPTION DRUG LABEL | 1 |