Clopidogrel
- Product NDC
- 50090-6568
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clopidogrel
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202928
- Marketing category
- ANDA
- Substance
- CLOPIDOGREL BISULFATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6568-0 | 90 TABLET in 1 BOTTLE (50090-6568-0) | 2023-07-28 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Clopidogrel | A-S Medication Solutions | 2024-09-29 | Human Prescription Drug Label | 4 |