# Rivaroxaban

NDC: 59651-849
Generic name: Rivaroxaban
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250410

FDA application: ANDA208544

## Active ingredients

- RIVAROXABAN: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-849"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-849
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bcb0e6e7-3006-4d82-8009-c5fddbbfc80d