Glipizide
- Product NDC
- 72162-2103
- 11-digit product format
- 721622103
- Labeler code
- 72162
- Product ID
- 72162-2103_ad1b0edd-91f2-4078-904d-340bae3c9eb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075795
- Marketing category
- ANDA
- Marketing start
- 2002-09-25
- 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 | 310490 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2103-0 | Glipizide | 1000 in 1 BOTTLE | TABLET | 1000 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2103 | GLIPIZIDE TABLET [BRYANT RANCH PREPACK] | 103 | Current NDC, 1 package rows | 20241011_560448dd-3690-43d9-9667-925f20bb816e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2103-0 | 72162210300 | 1000 TABLET in 1 BOTTLE (72162-2103-0) | 1000 tablet | 2002-09-25 | No | No | Historical |