# REBIF

NDC: 44087-0022
Generic name: INTERFERON BETA-1A
Labeler / Manufacturer: EMD Serono, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20020307

FDA application: BLA103780

## Active ingredients

- INTERFERON BETA-1A: 22 ug/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"44087-0022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=44087-0022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c6fcb5d2-8fcd-44fa-a838-b84ee5f44f0f