FDA NDC Directory · JSON-LD · Markdown

Tocilizumab-anoh

NDC 72606-050 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Generic nametocilizumab
Labeler / ManufacturerCELLTRION USA, Inc.
Marketing categoryBiologic License Application · App BLA761420
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsTOCILIZUMAB (400 mg/20mL)
Marketing started20250126
Package count2

External sources

Source: openFDA. Public-domain (CC0).