Glipizide
- Product NDC
- 51407-620
- 11-digit product format
- 514070620
- Labeler code
- 51407
- Product ID
- 51407-620_462b314b-adc2-201c-e063-6394a90a1c9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA074497
- Marketing category
- ANDA
- Marketing start
- 1995-08-31
- 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 |
|---|
| 51407-620-10 | Glipizide | 1000 in 1 BOTTLE | TABLET | 1000 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-620 | GLIPIZIDE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230325_d91d021f-f644-eac7-e053-2995a90a81c4.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 |
|---|
| 51407-620-10 | 51407062010 | 1000 TABLET in 1 BOTTLE (51407-620-10) | 1000 tablet | 2022-01-12 | 0000-00-00 | No | No | Current |