Glimepiride
- Product NDC
- 72189-485
- 11-digit product format
- 721890485
- Labeler code
- 72189
- Product ID
- 72189-485_2c4e2b74-1ef5-45c5-e063-6294a90af2b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA202759
- Marketing category
- ANDA
- Marketing start
- 2023-06-02
- Substance
- GLIMEPIRIDE
- Active strength
- 2 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 |
|---|
| 72189-485-30 | 72189048530 | 30 TABLET in 1 BOTTLE (72189-485-30) | 30 tablet | 2023-06-02 | No | No | Historical |
| 72189-485-60 | 72189048560 | 60 TABLET in 1 BOTTLE (72189-485-60) | 60 tablet | 2023-06-02 | No | No | Historical |
| 72189-485-90 | 72189048590 | 90 TABLET in 1 BOTTLE (72189-485-90) | 90 tablet | 2023-06-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Glimepiride | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 4 |