Fosinopril Sodium (Camber Pharmceuticals Inc.)
Welcome to the PulseAid listing for the Fosinopril Sodium drug offered from Camber Pharmceuticals 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: | Camber Pharmceuticals 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: | 2007-09-17 |
END MARKETING DATE: | 0000-00-00 |
Fosinopril Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Fosinopril Sodium from Camber Pharmceuticals Inc. |
LABELER NAME: | Camber Pharmceuticals Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/1) |
START MARKETING DATE: | 2007-09-17 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 31722-200_29914956-c794-4806-b038-f0784b9db3d3 |
PRODUCT NDC: | 31722-200 |
APPLICATION NUMBER: | ANDA077222 |
Other FOSINOPRIL SODIUM Pharmaceutical Manufacturers / Labelers: