Glipizide
- Product NDC
- 60687-690
- 11-digit product format
- 606870690
- Labeler code
- 60687
- Product ID
- 60687-690_237f3963-47ee-7dfa-e063-6394a90a6a1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075795
- Marketing category
- ANDA
- Marketing start
- 2023-05-26
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glipizide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLIPIZIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X7WDT95N5C |
| Rxcui | 310488, 310490 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-690-01 | Glipizide | 100 in 1 CARTON | TABLET | 100 | | 4 |
| 60687-690-11 | Glipizide | 1 in 1 BLISTER PACK | TABLET | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-690 | GLIPIZIDE TABLET [AMERICAN HEALTH PACKAGING] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241004_ff6805bb-b5f0-46d3-bf1d-3333b63ff1ae.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 |
|---|
| 60687-690-01 | 60687069001 | 100 BLISTER PACK in 1 CARTON (60687-690-01) / 1 TABLET in 1 BLISTER PACK (60687-690-11) | 100 blister pack | 2023-05-26 | 0000-00-00 | No | No | Current |
| 60687-690-11 | 60687069011 | 1 in 1 BLISTER PACK | | | | | | Historical |