Protriptyline hydrochloride (Hi-Tech Pharmacal Co., Inc.)
Welcome to the PulseAid listing for the Protriptyline hydrochloride drug offered from Hi-Tech Pharmacal Co., Inc.. This Tricyclic Antidepressant [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: | Hi-Tech Pharmacal Co., Inc. |
NON-PROPRIETARY NAME: | Protriptyline hydrochloride |
SUBSTANCE NAME: | PROTRIPTYLINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Tricyclic Antidepressant [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2013-10-28 |
END MARKETING DATE: | 0000-00-00 |
Protriptyline hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Protriptyline hydrochloride from Hi-Tech Pharmacal Co., Inc. |
LABELER NAME: | Hi-Tech Pharmacal Co., Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 2013-10-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 50383-959_9a773f26-2d86-4b5e-abfa-ef5718c8184b |
PRODUCT NDC: | 50383-959 |
APPLICATION NUMBER: | ANDA202220 |
Other PROTRIPTYLINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: