Simponi (Janssen Biotech, Inc.)


Welcome to the PulseAid listing for the Simponi 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: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2009-04-25
END MARKETING DATE: 0000-00-00


Simponi HUMAN PRESCRIPTION DRUG Details:

Item DescriptionSimponi from Janssen Biotech, Inc.
LABELER NAME: Janssen Biotech, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 50(mg/.5mL)
START MARKETING DATE: 2009-04-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57894-070_3387c121-c0fb-4721-bd4e-e61616f9bb83
PRODUCT NDC: 57894-070
APPLICATION NUMBER: BLA125289

Other GOLIMUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Janssen Biotech, Inc.Simponi