FDA NDC Directory · JSON-LD · Markdown

Hemlibra

NDC 50242-920 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameemicizumab
Labeler / ManufacturerGenentech, Inc.
Marketing categoryBiologic License Application · App BLA761083
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsEMICIZUMAB (30 mg/mL)
Marketing started20171116
Package count1

External sources

Source: openFDA. Public-domain (CC0).