Fosinopril Sodium and Hydrochlorothiazide (Heritage Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Fosinopril Sodium and Hydrochlorothiazide drug offered from Heritage Pharmaceuticals Inc.. 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: | Heritage Pharmaceuticals Inc. |
| NON-PROPRIETARY NAME: | Fosinopril Sodium and Hydrochlorothiazide Tablet |
| 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: | 2011-11-15 |
| END MARKETING DATE: | 0000-00-00 |
Fosinopril Sodium and Hydrochlorothiazide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Fosinopril Sodium and Hydrochlorothiazide from Heritage Pharmaceuticals Inc. |
| LABELER NAME: | Heritage Pharmaceuticals Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10; 12.5(mg/1; mg/1) |
| START MARKETING DATE: | 2011-11-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 23155-060_199837fb-147b-4251-a0db-08220c0d9045 |
| PRODUCT NDC: | 23155-060 |
| APPLICATION NUMBER: | ANDA079025 |
Other FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE Pharmaceutical Manufacturers / Labelers:
