REOPRO (Janssen Biotech, Inc.)
Welcome to the PulseAid listing for the REOPRO drug offered from Janssen Biotech, Inc.. This 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: | abciximab |
SUBSTANCE NAME: | ABCIXIMAB |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | BLA |
START MARKETING DATE: | 2017-01-03 |
END MARKETING DATE: | 0000-00-00 |
REOPRO HUMAN PRESCRIPTION DRUG Details:
Item Description | REOPRO from Janssen Biotech, Inc. |
LABELER NAME: | Janssen Biotech, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2(mg/mL) |
START MARKETING DATE: | 2017-01-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 57894-200_3e79eaa7-651f-4878-a2c7-e575f1cac040 |
PRODUCT NDC: | 57894-200 |
APPLICATION NUMBER: | BLA103575 |
Other ABCIXIMAB Pharmaceutical Manufacturers / Labelers: