Kineret (Swedish Orphan Biovitrum AB (publ))


Welcome to the PulseAid listing for the Kineret drug offered from Swedish Orphan Biovitrum AB (publ). This Interleukin 1 Receptor Antagonists [MoA],Interleukin-1 Receptor Antagonist [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Swedish Orphan Biovitrum AB (publ)
NON-PROPRIETARY NAME: anakinra
SUBSTANCE NAME: ANAKINRA
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Interleukin 1 Receptor Antagonists [MoA],Interleukin-1 Receptor Antagonist [EPC]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2009-12-15
END MARKETING DATE: 0000-00-00


Kineret HUMAN PRESCRIPTION DRUG Details:

Item DescriptionKineret from Swedish Orphan Biovitrum AB (publ)
LABELER NAME: Swedish Orphan Biovitrum AB (publ)
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/.67mL)
START MARKETING DATE: 2009-12-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66658-234_23568233-c1c2-4eb7-be9e-881cf32c85c5
PRODUCT NDC: 66658-234
APPLICATION NUMBER: BLA103950

Other ANAKINRA Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Swedish Orphan Biovitrum AB (publ)Kineret