FDA NDC Directory · JSON-LD · Markdown

Humira

NDC 0074-4339 · HUMAN PRESCRIPTION DRUG · KIT

Generic nameAdalimumab
Labeler / ManufacturerAbbVie Inc.
Marketing categoryBiologic License Application · App BLA125057
Dosage form / routeKIT
Active ingredients—
Marketing started20060623
Package count1

External sources

Source: openFDA. Public-domain (CC0).