FDA NDC Directory · JSON-LD · Markdown

Otulfi

NDC 65219-828 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameustekinumab-aauz
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryBiologic License Application · App BLA761379
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsUSTEKINUMAB (130 mg/26mL)
Marketing started20240222
Package count1

External sources

Source: openFDA. Public-domain (CC0).