Accupril (Parke-Davis Div of Pfizer Inc)
Welcome to the PulseAid listing for the Accupril drug offered from Parke-Davis Div of Pfizer 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: | Parke-Davis Div of Pfizer 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 |
START MARKETING DATE: | 1991-11-19 |
END MARKETING DATE: | 0000-00-00 |
Accupril HUMAN PRESCRIPTION DRUG Details:
Item Description | Accupril from Parke-Davis Div of Pfizer Inc |
LABELER NAME: | Parke-Davis Div of Pfizer Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 1991-11-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0071-0527_5bf68301-48f6-4c30-b27e-91e9a74dc5d0 |
PRODUCT NDC: | 0071-0527 |
APPLICATION NUMBER: | NDA019885 |
Other QUINAPRIL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: