Rivaroxaban
- Product NDC
- 50228-513
- 11-digit product format
- 502280513
- Labeler code
- 50228
- Product ID
- 50228-513_3b53cebf-946d-b82b-e063-6394a90a5da7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Rivaroxaban
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ScieGen pharmaceuticals,Inc
- Application
- ANDA218117
- Marketing category
- ANDA
- Marketing start
- 2025-08-04
- Substance
- RIVAROXABAN
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Factor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9NDF7JZ4M3 | RIVAROXABAN | 366789-02-8 | RIVAROXABAN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50228-513-18 | 50228051318 | 180 TABLET, FILM COATED in 1 BOTTLE (50228-513-18) | 2025-08-04 | No | No | Historical |
| 50228-513-60 | 50228051360 | 60 TABLET, FILM COATED in 1 BOTTLE (50228-513-60) | 2025-08-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rivaroxaban | ScieGen pharmaceuticals,Inc | 2025-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |