# ACTIMMUNE

NDC: 75987-111
Generic name: Interferon gamma-1b
Labeler / Manufacturer: Horizon Therapeutics USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20131201

FDA application: BLA103836

## Active ingredients

- INTERFERON GAMMA-1B: 100 ug/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75987-111"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75987-111
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5d0b1256-1981-4519-94f4-a4a2f98bd8a3