United States · FDA National Drug Code directory

UNLOXCYT

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
70095-130_32956dbc-6fe7-4e40-8496-cead92e453b7
Product NDC
70095-130
Form
INJECTION, SOLUTION
Composition / generic term
cosibelimab
Labeler
Sun Pharmaceutical Industries, Inc.
Marketing category
BLA
Marketing start / end (source format)
20251208
Source listing expiry
20261231

Source-listed ingredients

  • COSIBELIMAB — 300 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, GLASS in 1 CARTON (70095-130-01) / 5 mL in 1 VIAL, GLASS · 70095-130-01

Source and coverage

Open FDA National Drug Code directory

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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