Enoxaparin sodium (Winthrop U.S.)
Welcome to the PulseAid listing for the Enoxaparin sodium drug offered from Winthrop U.S.. This Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] 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: | Winthrop U.S. |
NON-PROPRIETARY NAME: | enoxaparin sodium |
SUBSTANCE NAME: | ENOXAPARIN SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC] |
ROUTE: | SUBCUTANEOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2011-10-03 |
END MARKETING DATE: | 0000-00-00 |
Enoxaparin sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Enoxaparin sodium from Winthrop U.S. |
LABELER NAME: | Winthrop U.S. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 30(mg/.3mL) |
START MARKETING DATE: | 2011-10-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0955-1003_8012fd96-8cbf-49d4-8e66-d4d1794ce080 |
PRODUCT NDC: | 0955-1003 |
APPLICATION NUMBER: | NDA020164 |
Other ENOXAPARIN SODIUM Pharmaceutical Manufacturers / Labelers: