Glipizide
- Product NDC
- 21695-469
- 11-digit product format
- 216950469
- Labeler code
- 21695
- Product ID
- 21695-469_e253ec37-78bb-4168-b630-2b7e33607f9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA074223
- Marketing category
- ANDA
- Marketing start
- 1995-02-27
- 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 |
|---|
| 21695-469-30 | Glipizide | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 21695-469-60 | Glipizide | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 21695-469-90 | Glipizide | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-469 | GLIPIZIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 3 package rows | 20110629_e253ec37-78bb-4168-b630-2b7e33607f9d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-469-30 | 21695046930 | 30 in 1 BOTTLE | Historical |
| 21695-469-60 | 21695046960 | 60 in 1 BOTTLE | Historical |
| 21695-469-90 | 21695046990 | 90 in 1 BOTTLE | Historical |