Glipizide
- Product NDC
- 72162-2614
- 11-digit product format
- 721622614
- Labeler code
- 72162
- Product ID
- 72162-2614_ae0ed781-abbb-4f3b-b52f-4cefc655ce03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206928
- Marketing category
- ANDA
- Marketing start
- 2023-03-03
- 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 | 315107 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2614-1 | Glipizide | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 100 |
| 72162-2614-5 | Glipizide | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2614-1 | 72162261401 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2614-1) | 2026-04-20 | No | No | Historical |
| 72162-2614-5 | 72162261405 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2614-5) | 2026-04-20 | No | No | Historical |