Ticagrelor
- Product NDC
- 0480-2688
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ticagrelor
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals, Inc.
- Application
- ANDA208390
- Marketing category
- ANDA
- Substance
- TICAGRELOR
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0480-2688-06 | 60 TABLET, FILM COATED in 1 BOTTLE (0480-2688-06) | 2025-05-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ticagrelor | Teva Pharmaceuticals, Inc. | 2024-12-20 | HUMAN PRESCRIPTION DRUG LABEL | 2 |