OPDIVO (E.R. Squibb & Sons, L.L.C.)


Welcome to the PulseAid listing for the OPDIVO drug offered from E.R. Squibb & Sons, L.L.C.. This Programmed Death Receptor-1 Blocking Antibody [EPC],Programmed Death Receptor-1-directed Antibody Interactions [MoA] 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: E.R. Squibb & Sons, L.L.C.
NON-PROPRIETARY NAME: nivolumab
SUBSTANCE NAME: NIVOLUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Programmed Death Receptor-1 Blocking Antibody [EPC],Programmed Death Receptor-1-directed Antibody Interactions [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2014-12-22
END MARKETING DATE: 0000-00-00


OPDIVO HUMAN PRESCRIPTION DRUG Details:

Item DescriptionOPDIVO from E.R. Squibb & Sons, L.L.C.
LABELER NAME: E.R. Squibb & Sons, L.L.C.
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/mL)
START MARKETING DATE: 2014-12-22
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0003-3772_aeb6b7b2-544b-430b-a736-9f8b08d19c6c
PRODUCT NDC: 0003-3772
APPLICATION NUMBER: BLA125554

Other NIVOLUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
E.R. Squibb & Sons, L.L.C.OPDIVO