Protriptyline Hydrochloride (Rising Pharmaceuticals, Inc)


Welcome to the PulseAid listing for the Protriptyline Hydrochloride drug offered from Rising Pharmaceuticals, 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: Rising Pharmaceuticals, 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: 2010-06-11
END MARKETING DATE: 0000-00-00


Protriptyline Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionProtriptyline Hydrochloride from Rising Pharmaceuticals, Inc
LABELER NAME: Rising Pharmaceuticals, Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 5(mg/1)
START MARKETING DATE: 2010-06-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 64980-158_cfa7bf92-274c-478e-ad74-910fa7d21512
PRODUCT NDC: 64980-158
APPLICATION NUMBER: ANDA090462

Other PROTRIPTYLINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Epic Pharma, LLCProtriptyline Hydrochloride
Hi-Tech Pharmacal Co., Inc.Protriptyline hydrochloride
Rising Pharmaceuticals, IncProtriptyline Hydrochloride
West-Ward Pharmaceuticals Corp.Protriptyline Hydrochloride