FDA NDC Directory · JSON-LD · Markdown

Adalimumab-aacf

NDC 65219-620 · HUMAN PRESCRIPTION DRUG · KIT

Generic nameadalimumab
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryBiologic License Application · App BLA761255
Dosage form / routeKIT · SUBCUTANEOUS
Active ingredients—
Marketing started20240630
Package count1

External sources

Source: openFDA. Public-domain (CC0).