Cesamet (Valeant Pharmaceuticals North America)


Welcome to the PulseAid listing for the Cesamet drug offered from Valeant Pharmaceuticals North America. This Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient] 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: Valeant Pharmaceuticals North America
NON-PROPRIETARY NAME: NABILONE
SUBSTANCE NAME: NABILONE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2009-11-01
END MARKETING DATE: 0000-00-00


Cesamet HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCesamet from Valeant Pharmaceuticals North America
LABELER NAME: Valeant Pharmaceuticals North America
DEA SCHEDULE: CII
ACTIVE STRENGTH: 1(mg/1)
START MARKETING DATE: 2009-11-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0187-1221_01c46f44-14ff-4510-89cb-84114ce439de
PRODUCT NDC: 0187-1221
APPLICATION NUMBER: NDA018677

Other NABILONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Meda Pharmaceuticals Inc.Cesamet
Valeant Pharmaceuticals North AmericaCesamet