United States · FDA National Drug Code directory
ACTIMMUNE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 75987-111_8d803fd6-c715-4d8b-818b-bd5d537c3d60
- Product NDC
- 75987-111
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Interferon gamma-1b
- Labeler
- Horizon Therapeutics USA, Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 20131201
- Source listing expiry
- 20271231
Source-listed ingredients
- INTERFERON GAMMA-1B — 100 ug/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 VIAL, SINGLE-DOSE in 1 CARTON (75987-111-11) / .5 mL in 1 VIAL, SINGLE-DOSE (75987-111-10) · 75987-111-11
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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