Quinapril Hydrochloride (Greenstone LLC)
Welcome to the PulseAid listing for the Quinapril Hydrochloride drug offered from Greenstone LLC. 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: | Greenstone LLC |
| 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: | 2018-05-31 |
Quinapril Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Quinapril Hydrochloride from Greenstone LLC |
| LABELER NAME: | Greenstone LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20(mg/1) |
| START MARKETING DATE: | 1991-11-19 |
| END MARKETING DATE: | 2018-05-31 |
| PRODUCT ID: | 59762-5021_982b4358-b016-4351-9fda-38d8c42dcf72 |
| PRODUCT NDC: | 59762-5021 |
| APPLICATION NUMBER: | NDA019885 |
Other QUINAPRIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
