Glipizide
- Product NDC
- 50090-2075
- 11-digit product format
- 500902075
- Labeler code
- 50090
- Product ID
- 50090-2075_e8b79b32-8563-455d-bd72-367ce9f4d992
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074550
- Marketing category
- ANDA
- Marketing start
- 2011-07-18
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-2075-0 | EA - Each | 50090-2075 | 9c03fbb1-a7a4-4fa9-b317-ea02d4f7d7a7 | 1 | 2019-02-13 |
| 50090-2075-1 | EA - Each | 50090-2075 | 5c8ece9d-2c50-4640-a703-2d655a59e59a | 1 | 2018-11-06 |
| 50090-2075-2 | EA - Each | 50090-2075 | 21595ed8-ae6b-4ef9-8eee-3db134a9b40f | 1 | 2018-11-06 |
| 50090-2075-4 | EA - Each | 50090-2075 | 315d50c3-b1df-4ff3-abf1-8863576e3b55 | 1 | 2019-02-13 |
| 50090-2075-5 | EA - Each | 50090-2075 | 6ecf85ef-9b1e-448e-b314-2785f85a1108 | 1 | 2018-11-06 |
| 50090-2075-6 | EA - Each | 50090-2075 | c1d0621f-1533-477c-b842-fd0e12be7ddd | 1 | 2018-11-06 |