FDA NDC Directory · JSON-LD · Markdown

TREMFYA

NDC 57894-640 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameGuselkumab
Labeler / ManufacturerJanssen Biotech, Inc.
Marketing categoryBiologic License Application · App BLA761061
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsGUSELKUMAB (100 mg/mL)
Marketing started20170713
Package count5

External sources

Source: openFDA. Public-domain (CC0).