Glimepiride
- Product NDC
- 71205-773
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glimepiride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA202759
- Marketing category
- ANDA
- Substance
- GLIMEPIRIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-773-30 | 30 TABLET in 1 BOTTLE (71205-773-30) | 2023-03-13 | | No | Historical |
| 71205-773-60 | 60 TABLET in 1 BOTTLE (71205-773-60) | 2023-03-13 | | No | Historical |
| 71205-773-78 | 180 TABLET in 1 BOTTLE (71205-773-78) | 2023-03-13 | | No | Historical |
| 71205-773-90 | 90 TABLET in 1 BOTTLE (71205-773-90) | 2023-03-13 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Glimepiride | Proficient Rx LP | 2023-03-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |