Rivaroxaban 51672-4228
Product NDC
51672-4228- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 15, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA208557
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Rivaroxaban | 2.5 mg/1 |
Drug Class
Factor Xa Inhibitor [EPC]Factor Xa Inhibitor [EPC]Factor Xa Inhibitors [MoA]
Packaging Options(2)
60 TABLET, COATED in 1 BOTTLE (51672-4228-4)
180 TABLET, COATED in 1 BOTTLE (51672-4228-9)