Venofer (American Regent, Inc.)
Welcome to the PulseAid listing for the Venofer drug offered from American Regent, Inc.. This Iron [Chemical/Ingredient],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [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: | American Regent, Inc. |
NON-PROPRIETARY NAME: | iron sucrose |
SUBSTANCE NAME: | IRON SUCROSE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Iron [Chemical/Ingredient],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2007-06-12 |
END MARKETING DATE: | 0000-00-00 |
Venofer HUMAN PRESCRIPTION DRUG Details:
Item Description | Venofer from American Regent, Inc. |
LABELER NAME: | American Regent, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20(mg/mL) |
START MARKETING DATE: | 2007-06-12 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0517-2310_cff8fa5e-41df-4fa6-b7f3-0c46168af38f |
PRODUCT NDC: | 0517-2310 |
APPLICATION NUMBER: | NDA021135 |
Other IRON SUCROSE Pharmaceutical Manufacturers / Labelers: