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 DescriptionAnzemet from sanofi-aventis U.S. LLC
LABELER NAME: sanofi-aventis U.S. LLC
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Avera McKennan HospitalANZEMET
sanofi-aventis U.S. LLCAnzemet
Validus Pharmaceuticals LLCANZEMET