Dutasteride (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Dutasteride drug offered from Actavis Pharma, Inc.. This 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase 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: | Actavis Pharma, Inc. |
NON-PROPRIETARY NAME: | Dutasteride |
SUBSTANCE NAME: | DUTASTERIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-11-20 |
END MARKETING DATE: | 0000-00-00 |
Dutasteride HUMAN PRESCRIPTION DRUG Details:
Item Description | Dutasteride from Actavis Pharma, Inc. |
LABELER NAME: | Actavis Pharma, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/1) |
START MARKETING DATE: | 2015-11-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0591-2292_35dc50da-d6ec-45c9-9da6-2eff55c929ea |
PRODUCT NDC: | 0591-2292 |
APPLICATION NUMBER: | ANDA202808 |
Other DUTASTERIDE Pharmaceutical Manufacturers / Labelers: