DUTASTERIDE (Breckenridge Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the DUTASTERIDE drug offered from Breckenridge Pharmaceutical, 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: | Breckenridge Pharmaceutical, 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 Breckenridge Pharmaceutical, Inc. |
LABELER NAME: | Breckenridge Pharmaceutical, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 0.5(mg/1) |
START MARKETING DATE: | 2015-11-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51991-749_3c751a2d-04d6-4362-8f0d-c64428793e99 |
PRODUCT NDC: | 51991-749 |
APPLICATION NUMBER: | ANDA204705 |
Other DUTASTERIDE Pharmaceutical Manufacturers / Labelers: