Dupixent (sanofi-aventis U.S. LLC)


Welcome to the PulseAid listing for the Dupixent drug offered from sanofi-aventis U.S. LLC. This Interleukin-4 Receptor alpha Antagonist [EPC],Interleukin 4 Receptor alpha Antagonists [MoA],Antibodies, Monoclonal [Chemical/Ingredient] 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: sanofi-aventis U.S. LLC
NON-PROPRIETARY NAME: Dupilumab
SUBSTANCE NAME: DUPILUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Interleukin-4 Receptor alpha Antagonist [EPC],Interleukin 4 Receptor alpha Antagonists [MoA],Antibodies, Monoclonal [Chemical/Ingredient]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2017-03-28
END MARKETING DATE: 0000-00-00


Dupixent HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDupixent from sanofi-aventis U.S. LLC
LABELER NAME: sanofi-aventis U.S. LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 300(mg/2mL)
START MARKETING DATE: 2017-03-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0024-5914_e23c3c02-6f3f-425f-925a-781b74e979bc
PRODUCT NDC: 0024-5914
APPLICATION NUMBER: BLA761055

Other DUPILUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
sanofi-aventis U.S. LLCDupixent