Quinapril Hydrochloride (PD-Rx Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Quinapril Hydrochloride drug offered from PD-Rx Pharmaceuticals, Inc.. This Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme 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: | PD-Rx Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | quinapril hydrochloride |
SUBSTANCE NAME: | QUINAPRIL HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 1991-11-19 |
END MARKETING DATE: | 0000-00-00 |
Quinapril Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Quinapril Hydrochloride from PD-Rx Pharmaceuticals, Inc. |
LABELER NAME: | PD-Rx Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/1) |
START MARKETING DATE: | 1991-11-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 43063-358_559f78de-f11c-42d8-e054-00144ff88e88 |
PRODUCT NDC: | 43063-358 |
APPLICATION NUMBER: | NDA019885 |
Other QUINAPRIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: