Fosinopril sodium (Exelan Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Fosinopril sodium drug offered from Exelan Pharmaceuticals, 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: | Exelan Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | Fosinopril sodium |
| SUBSTANCE NAME: | FOSINOPRIL SODIUM |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2005-06-21 |
| END MARKETING DATE: | 0000-00-00 |
Fosinopril sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Fosinopril sodium from Exelan Pharmaceuticals, Inc. |
| LABELER NAME: | Exelan Pharmaceuticals, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 2005-06-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 76282-200_1e8b9703-41f2-4ce0-963f-0aedc48db2eb |
| PRODUCT NDC: | 76282-200 |
| APPLICATION NUMBER: | ANDA077222 |
Other FOSINOPRIL SODIUM Pharmaceutical Manufacturers / Labelers:
