Fosinopril Sodium and Hydrochlorothiazide (Bryant Ranch Prepack)
Welcome to the PulseAid listing for the Fosinopril Sodium and Hydrochlorothiazide drug offered from Bryant Ranch Prepack. This Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] 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: | Bryant Ranch Prepack |
NON-PROPRIETARY NAME: | Fosinopril Sodium and Hydrochlorothiazide |
SUBSTANCE NAME: | FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2009-07-09 |
END MARKETING DATE: | 0000-00-00 |
Fosinopril Sodium and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
Item Description | Fosinopril Sodium and Hydrochlorothiazide from Bryant Ranch Prepack |
LABELER NAME: | Bryant Ranch Prepack |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10; 12.5(mg/1; mg/1) |
START MARKETING DATE: | 2009-07-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63629-6993_9be85a63-ddd3-483b-8e2e-6549c0e0793f |
PRODUCT NDC: | 63629-6993 |
APPLICATION NUMBER: | ANDA079245 |
Other FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers: