FDA NDC Directory · JSON-LD · Markdown

Humira

NDC 83457-554 · HUMAN PRESCRIPTION DRUG · KIT

Generic nameAdalimumab
Labeler / ManufacturerCordavis Limited
Marketing categoryBiologic License Application · App BLA125057
Dosage form / routeKIT
Active ingredients—
Marketing started20240214
Package count1

External sources

Source: openFDA. Public-domain (CC0).