Quinapril (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the Quinapril drug offered from Sun Pharmaceutical Industries Limited. 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: | Sun Pharmaceutical Industries Limited |
| NON-PROPRIETARY NAME: | Quinapril |
| 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: | ANDA |
| START MARKETING DATE: | 2009-06-18 |
| END MARKETING DATE: | 0000-00-00 |
Quinapril HUMAN PRESCRIPTION DRUG Details:
| Item Description | Quinapril from Sun Pharmaceutical Industries Limited |
| LABELER NAME: | Sun Pharmaceutical Industries Limited |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/1) |
| START MARKETING DATE: | 2009-06-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62756-310_461bf92c-0ad0-4e99-8542-6dc6bfbde5f1 |
| PRODUCT NDC: | 62756-310 |
| APPLICATION NUMBER: | ANDA090800 |
Other QUINAPRIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
