Glipizide
- Product NDC
- 10544-193
- 11-digit product format
- 105440193
- Labeler code
- 10544
- Product ID
- 10544-193_11f93c9c-792a-3add-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 2012-01-18
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10544-193-60 | Glipizide | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-193 | GLIPIZIDE TABLET [BLENHEIM PHARMACAL, INC.] | 3 | Legacy NDC, 1 package rows | 20150323_3030da52-4e59-44d0-9d62-4b27e38e7e91.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-193-60 | 10544019360 | 60 in 1 BOTTLE | Historical |