Ticagrelor
- Product NDC
- 62332-500
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ticagrelor
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Alembic Pharmaceuticals Inc.
- Application
- ANDA208576
- Marketing category
- ANDA
- Substance
- TICAGRELOR
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 62332-500-60 | 60 TABLET, FILM COATED in 1 BOTTLE (62332-500-60) | 2025-10-28 | | No | Historical |
| 62332-500-71 | 500 TABLET, FILM COATED in 1 BOTTLE (62332-500-71) | 2025-10-28 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ticagrelor | Alembic Pharmaceuticals Inc. | Alembic Pharmaceuticals Limited | 2025-10-30 | Human Prescription Drug Label | 19 |
| Ticagrelor | Alembic Pharmaceuticals Inc. | Alembic Pharmaceuticals Limited | 2025-05-07 | Human Prescription Drug Label | 18 |