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 Description | SIMPONI ARIA from Janssen Biotech, Inc. |
LABELER NAME: | Janssen Biotech, Inc. |
DEA SCHEDULE: |
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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: