Glipizide
- Product NDC
- 68645-575
- 11-digit product format
- 686450575
- Labeler code
- 68645
- Product ID
- 68645-575_4c224fbc-84ca-04c5-e063-6394a90a4458
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA075795
- Marketing category
- ANDA
- Marketing start
- 2002-09-25
- Substance
- GLIPIZIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glipizide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLIPIZIDE | 10 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 |
|---|
| 68645-575-59 | Glipizide | 60 in 1 BOTTLE | TABLET | 60 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68645-575 | GLIPIZIDE TABLET [LEGACY PHARMACEUTICAL PACKAGING, LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250321_116ffc6a-735c-49e0-a9d5-69b6bc3e3706.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 |
|---|
| 68645-575-59 | 68645057559 | 60 TABLET in 1 BOTTLE (68645-575-59) | 60 tablet | 2002-09-25 | 0000-00-00 | No | No | Current |