Fosinopril Sodium (Eon Labs, Inc.)
Welcome to the PulseAid listing for the Fosinopril Sodium drug offered from Eon Labs, 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: | Eon Labs, 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: | 2004-04-23 |
| END MARKETING DATE: | 0000-00-00 |
Fosinopril Sodium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Fosinopril Sodium from Eon Labs, Inc. |
| LABELER NAME: | Eon Labs, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 2004-04-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0185-0041_2fea746d-9480-455d-a2e0-8ec35fafe736 |
| PRODUCT NDC: | 0185-0041 |
| APPLICATION NUMBER: | ANDA076483 |
Other FOSINOPRIL SODIUM Pharmaceutical Manufacturers / Labelers:
