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 Description | Dupixent from sanofi-aventis U.S. LLC |
LABELER NAME: | sanofi-aventis U.S. LLC |
DEA SCHEDULE: |
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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: