Galantamine (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Galantamine drug offered from Teva Pharmaceuticals USA, Inc.. 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: | Teva Pharmaceuticals USA, Inc. |
NON-PROPRIETARY NAME: | Galantamine |
SUBSTANCE NAME: | GALANTAMINE HYDROBROMIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2008-08-28 |
END MARKETING DATE: | 2018-01-31 |
Galantamine HUMAN PRESCRIPTION DRUG Details:
Item Description | Galantamine from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 4(mg/1) |
START MARKETING DATE: | 2008-08-28 |
END MARKETING DATE: | 2018-01-31 |
PRODUCT ID: | 0555-0138_86a1c2ed-fde6-483a-802f-386cb134ad40 |
PRODUCT NDC: | 0555-0138 |
APPLICATION NUMBER: | ANDA077605 |
Other GALANTAMINE HYDROBROMIDE Pharmaceutical Manufacturers / Labelers: