Glyburide
- Product NDC
- 71335-2771
- 11-digit product format
- 713352771
- Labeler code
- 71335
- Product ID
- 71335-2771_ce71c7bb-a31a-4b76-8d0c-d717e8eeda9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glyburide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203379
- Marketing category
- ANDA
- Marketing start
- 2021-10-05
- Substance
- GLYBURIDE
- 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
- Glyburide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GLYBURIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SX6K58TVWC |
| Rxcui | 310537 |
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 |
|---|
| 71335-2771-1 | 71335277101 | 30 TABLET in 1 BOTTLE (71335-2771-1) | 30 tablet | 2025-10-03 | No | No | Current |
| 71335-2771-2 | 71335277102 | 120 TABLET in 1 BOTTLE (71335-2771-2) | 120 tablet | 2025-10-03 | No | No | Current |
| 71335-2771-3 | 71335277103 | 100 TABLET in 1 BOTTLE (71335-2771-3) | 100 tablet | 2025-10-03 | No | No | Current |
| 71335-2771-4 | 71335277104 | 60 TABLET in 1 BOTTLE (71335-2771-4) | 60 tablet | 2025-10-03 | No | No | Current |
| 71335-2771-5 | 71335277105 | 90 TABLET in 1 BOTTLE (71335-2771-5) | 90 tablet | 2025-10-03 | No | No | Current |
| 71335-2771-6 | 71335277106 | 180 TABLET in 1 BOTTLE (71335-2771-6) | 180 tablet | 2025-10-03 | No | No | Current |