Glipizide
- Product NDC
- 68788-4061
- 11-digit product format
- 687884061
- Labeler code
- 68788
- Product ID
- 68788-4061_410bf280-838d-45af-9b60-15f94ded7581
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA074378
- Marketing category
- ANDA
- Marketing start
- 2026-01-28
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-4061-1 | 68788406101 | 100 TABLET in 1 BOTTLE (68788-4061-1) | 100 tablet | 2026-01-28 | No | No | Historical |
| 68788-4061-3 | 68788406103 | 30 TABLET in 1 BOTTLE (68788-4061-3) | 30 tablet | 2026-01-28 | No | No | Historical |
| 68788-4061-6 | 68788406106 | 60 TABLET in 1 BOTTLE (68788-4061-6) | 60 tablet | 2026-01-28 | No | No | Historical |
| 68788-4061-8 | 68788406108 | 180 TABLET in 1 BOTTLE (68788-4061-8) | 180 tablet | 2026-01-28 | No | No | Historical |
| 68788-4061-9 | 68788406109 | 90 TABLET in 1 BOTTLE (68788-4061-9) | 90 tablet | 2026-01-28 | No | No | Historical |