Glipizide
- Product NDC
- 68071-2839
- 11-digit product format
- 680712839
- Labeler code
- 68071
- Product ID
- 68071-2839_f1775df0-5272-38ca-e053-2a95a90a73c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA074497
- Marketing category
- ANDA
- Marketing start
- 2021-12-13
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2839-6 | Glipizide | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 68071-2839-8 | Glipizide | 180 in 1 BOTTLE | TABLET | 180 | | 3 |
| 68071-2839-9 | Glipizide | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2839 | GLIPIZIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 3 | Legacy NDC, 3 package rows | 20230106_ed9a649a-1acd-ec8a-e053-2a95a90a43da.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2839-6 | 68071283906 | 60 TABLET in 1 BOTTLE (68071-2839-6) | 60 tablet | 2023-01-04 | 0000-00-00 | No | No | Current |
| 68071-2839-8 | 68071283908 | 180 TABLET in 1 BOTTLE (68071-2839-8) | 180 tablet | 2022-11-16 | 0000-00-00 | No | No | Current |
| 68071-2839-9 | 68071283909 | 90 TABLET in 1 BOTTLE (68071-2839-9) | 90 tablet | 2022-11-16 | 0000-00-00 | No | No | Current |