Simulect (Novartis Pharmaceuticals Corporation)


Welcome to the PulseAid listing for the Simulect drug offered from Novartis Pharmaceuticals Corporation. This Interleukin 2 Receptor Antagonists [MoA],Interleukin 2 Receptor-directed Antibody Interactions [MoA],Interleukin-2 Receptor Blocking Antibody [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: Novartis Pharmaceuticals Corporation
NON-PROPRIETARY NAME: basiliximab
SUBSTANCE NAME: BASILIXIMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Interleukin 2 Receptor Antagonists [MoA],Interleukin 2 Receptor-directed Antibody Interactions [MoA],Interleukin-2 Receptor Blocking Antibody [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, FOR SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 1998-05-12
END MARKETING DATE: 0000-00-00


Simulect HUMAN PRESCRIPTION DRUG Details:

Item DescriptionSimulect from Novartis Pharmaceuticals Corporation
LABELER NAME: Novartis Pharmaceuticals Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 20(mg/5mL)
START MARKETING DATE: 1998-05-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0078-0331_88e1d8f7-be69-4d69-b417-0125a8a6b4b9
PRODUCT NDC: 0078-0331
APPLICATION NUMBER: BLA103764

Other BASILIXIMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Novartis Pharmaceuticals CorporationSimulect