FDA NDC Directory · JSON-LD · Markdown

TREMFYA

NDC 57894-651 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameguselkumab
Labeler / ManufacturerJanssen Biotech, Inc.
Marketing categoryBiologic License Application · App BLA761061
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsGUSELKUMAB (200 mg/2mL)
Marketing started20240911
Package count4

External sources

Source: openFDA. Public-domain (CC0).