SIMPONI ARIA (Janssen Biotech, Inc.)


Welcome to the PulseAid listing for the SIMPONI ARIA 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: golimumab
SUBSTANCE NAME: GOLIMUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Tumor Necrosis Factor Blocker [EPC],Tumor Necrosis Factor Receptor Blocking Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2013-07-19
END MARKETING DATE: 0000-00-00


SIMPONI ARIA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionSIMPONI ARIA from Janssen Biotech, Inc.
LABELER NAME: Janssen Biotech, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 50(mg/4mL)
START MARKETING DATE: 2013-07-19
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57894-350_c768f495-1a81-4956-9494-80e768262117
PRODUCT NDC: 57894-350
APPLICATION NUMBER: BLA125433

Other GOLIMUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Janssen Biotech, Inc.Simponi