FDA NDC Directory · JSON-LD · Markdown

Riabni

NDC 55513-326 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namerituximab-arrx
Labeler / ManufacturerAmgen, Inc
Marketing categoryBiologic License Application · App BLA761140
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsRITUXIMAB (500 mg/50mL)
Marketing started20210106
Package count2

External sources

Source: openFDA. Public-domain (CC0).