Anzemet (sanofi-aventis U.S. LLC)
Welcome to the PulseAid listing for the Anzemet drug offered from sanofi-aventis U.S. LLC. This Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] 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: | sanofi-aventis U.S. LLC |
NON-PROPRIETARY NAME: | dolasetron mesylate |
SUBSTANCE NAME: | DOLASETRON MESYLATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1997-09-11 |
END MARKETING DATE: | 0000-00-00 |
Anzemet HUMAN PRESCRIPTION DRUG Details:
Item Description | Anzemet from sanofi-aventis U.S. LLC |
LABELER NAME: | sanofi-aventis U.S. LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 100(mg/5mL) |
START MARKETING DATE: | 1997-09-11 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0088-1206_9a32e15f-3a74-4fd6-934f-58f94836be80 |
PRODUCT NDC: | 0088-1206 |
APPLICATION NUMBER: | NDA020624 |
Other DOLASETRON MESYLATE Pharmaceutical Manufacturers / Labelers: