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TYENNE

NDC 65219-590 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Generic nameTocilizumab-aazg
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryBiologic License Application · App BLA761275
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsTOCILIZUMAB (80 mg/4mL)
Marketing started20240415
Package count1

External sources

Source: openFDA. Public-domain (CC0).