Glipizide
- Product NDC
- 67296-0894
- 11-digit product format
- 672960894
- Labeler code
- 67296
- Product ID
- 67296-0894_9c9af9a6-90ba-2d61-e053-2a95a90afcbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA074305
- Marketing category
- ANDA
- Marketing start
- 1995-04-07
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 67296-0894-1 | Glipizide | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0894 | GLIPIZIDE TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20200121_4dae3b5e-c44f-3de5-e054-00144ff8d46c.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 |
|---|
| 67296-0894-1 | 67296089401 | 30 TABLET in 1 BOTTLE (67296-0894-1) | 30 tablet | 1995-04-07 | 0000-00-00 | No | No | Current |