Prazosin Hydrochloride (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Prazosin Hydrochloride drug offered from Teva Pharmaceuticals USA, Inc.. This Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] 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: | Prazosin Hydrochloride |
SUBSTANCE NAME: | PRAZOSIN HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2007-02-22 |
END MARKETING DATE: | 0000-00-00 |
Prazosin Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Prazosin Hydrochloride from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 1(mg/1) |
START MARKETING DATE: | 2007-02-22 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0093-4067_f7e4a650-7b7b-41dd-b163-7d8857251fc3 |
PRODUCT NDC: | 0093-4067 |
APPLICATION NUMBER: | ANDA071745 |
Other PRAZOSIN HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: