Exelon (Novartis Pharmaceuticals Corporation)
Welcome to the PulseAid listing for the Exelon drug offered from Novartis Pharmaceuticals Corporation. This Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] 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: | Novartis Pharmaceuticals Corporation |
NON-PROPRIETARY NAME: | rivastigmine tartrate |
SUBSTANCE NAME: | RIVASTIGMINE TARTRATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2000-04-30 |
END MARKETING DATE: | 0000-00-00 |
Exelon HUMAN PRESCRIPTION DRUG Details:
Item Description | Exelon from Novartis Pharmaceuticals Corporation |
LABELER NAME: | Novartis Pharmaceuticals Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1.5(mg/1) |
START MARKETING DATE: | 2000-04-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0078-0323_995e8f94-ac01-4921-a7fd-fac1d68adc2f |
PRODUCT NDC: | 0078-0323 |
APPLICATION NUMBER: | NDA020823 |
Other RIVASTIGMINE TARTRATE Pharmaceutical Manufacturers / Labelers: