REMICADE (Janssen Biotech, Inc.)


Welcome to the PulseAid listing for the REMICADE drug offered from Janssen Biotech, Inc.. This Tumor Necrosis Factor Blocker [EPC],Tumor Necrosis Factor Receptor Blocking Activity [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: Janssen Biotech, Inc.
NON-PROPRIETARY NAME: INFLIXIMAB
SUBSTANCE NAME: INFLIXIMAB, LICENSE HOLDER UNSPECIFIED
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Tumor Necrosis Factor Blocker [EPC],Tumor Necrosis Factor Receptor Blocking Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 1998-08-24
END MARKETING DATE: 0000-00-00


REMICADE HUMAN PRESCRIPTION DRUG Details:

Item DescriptionREMICADE from Janssen Biotech, Inc.
LABELER NAME: Janssen Biotech, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/10mL)
START MARKETING DATE: 1998-08-24
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57894-030_dd84d623-c0c3-4783-9f5e-3b71c818bfd3
PRODUCT NDC: 57894-030
APPLICATION NUMBER: BLA103772

Other INFLIXIMAB, LICENSE HOLDER UNSPECIFIED Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Janssen Biotech, Inc.REMICADE
Pfizer Laboratories Div Pfizer IncINFLECTRA