Glipizide
- Product NDC
- 53217-317
- 11-digit product format
- 532170317
- Labeler code
- 53217
- Product ID
- 53217-317_79b13115-7269-4058-95f3-8403ecdc0d5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA074550
- Marketing category
- ANDA
- Marketing start
- 2011-07-18
- 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
- 2019-12-31
- 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 |
|---|
| 53217-317-30 | Glipizide | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 53217-317-90 | Glipizide | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
| 53217-317-99 | Glipizide | 180 in 1 BOTTLE | TABLET | 180 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-317 | GLIPIZIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20170525_b545266d-9d05-4d7d-993f-df36592751e4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-317-30 | 53217031730 | 30 in 1 BOTTLE | Historical |
| 53217-317-90 | 53217031790 | 90 in 1 BOTTLE | Historical |
| 53217-317-99 | 53217031799 | 180 in 1 BOTTLE | Historical |