Glipizide
- Product NDC
- 71335-1042
- 11-digit product format
- 713351042
- Labeler code
- 71335
- Product ID
- 71335-1042_b2e42e92-1292-4d1e-b235-6e252e708b1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204720
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Substance
- GLIPIZIDE
- Active strength
- 2.5 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 | 2.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X7WDT95N5C |
| Rxcui | 310489, 314006, 315107 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-1042-1 | Glipizide | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 8 |
| 71335-1042-2 | Glipizide | 60 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 60 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1042 | GLIPIZIDE TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK] | 8 | Current NDC, Legacy NDC, 2 package rows | 20241222_0338aff9-29f9-405e-b516-06ef4b863863.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1042-1 | 71335104201 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1042-1) | 2019-01-08 | 0000-00-00 | No | No | Current |
| 71335-1042-2 | 71335104202 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1042-2) | 2019-01-08 | 0000-00-00 | No | No | Current |