# Truxima

NDC: 63459-103
Generic name: rituximab-abbs
Labeler / Manufacturer: Cephalon, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200504

FDA application: BLA761088

## Active ingredients

- RITUXIMAB: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63459-103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63459-103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9af3ddc7-4217-417a-ac89-8704edc5bc44