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Kineret

NDC 66658-234 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameanakinra
Labeler / ManufacturerSwedish Orphan Biovitrum AB (publ)
Marketing categoryBiologic License Application · App BLA103950
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsANAKINRA (100 mg/.67mL)
Marketing started20091215
Package count2

External sources

Source: openFDA. Public-domain (CC0).