Glimepiride
- Product NDC
- 71335-2409
- 11-digit product format
- 713352409
- Labeler code
- 71335
- Product ID
- 71335-2409_5f8f3cde-9b59-4f0a-8363-2a645e3b904d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202112
- Marketing category
- ANDA
- Marketing start
- 2023-07-31
- Substance
- GLIMEPIRIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6KY687524K | GLIMEPIRIDE | 93479-97-1 | GLIMEPIRIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2409-1 | 71335240901 | 30 TABLET in 1 BOTTLE (71335-2409-1) | 30 tablet | 2024-06-11 | No | No | Historical |
| 71335-2409-2 | 71335240902 | 60 TABLET in 1 BOTTLE (71335-2409-2) | 60 tablet | 2024-06-11 | No | No | Historical |
| 71335-2409-3 | 71335240903 | 90 TABLET in 1 BOTTLE (71335-2409-3) | 90 tablet | 2024-06-11 | No | No | Historical |
| 71335-2409-4 | 71335240904 | 180 TABLET in 1 BOTTLE (71335-2409-4) | 180 tablet | 2024-06-11 | No | No | Historical |
| 71335-2409-5 | 71335240905 | 100 TABLET in 1 BOTTLE (71335-2409-5) | 100 tablet | 2024-06-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Glimepiride | Bryant Ranch Prepack | 2024-06-11 | HUMAN PRESCRIPTION DRUG LABEL | 1 |