SYNRIBO (Cephalon, Inc.)
Welcome to the PulseAid listing for the SYNRIBO drug offered from Cephalon, 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: | Cephalon, Inc. |
NON-PROPRIETARY NAME: | Omacetaxine Mepesuccinate |
SUBSTANCE NAME: | OMACETAXINE MEPESUCCINATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | SUBCUTANEOUS |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2012-11-19 |
END MARKETING DATE: | 0000-00-00 |
SYNRIBO HUMAN PRESCRIPTION DRUG Details:
Item Description | SYNRIBO from Cephalon, Inc. |
LABELER NAME: | Cephalon, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3.5(mg/mL) |
START MARKETING DATE: | 2012-11-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63459-177_ac6c18d2-3fea-42f8-8ce7-20019b6c622e |
PRODUCT NDC: | 63459-177 |
APPLICATION NUMBER: | NDA203585 |
Other OMACETAXINE MEPESUCCINATE Pharmaceutical Manufacturers / Labelers: