Heparin Sodium (Sandoz Inc)
Welcome to the PulseAid listing for the Heparin Sodium drug offered from Sandoz Inc. This Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated 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: | Sandoz Inc |
NON-PROPRIETARY NAME: | Heparin Sodium |
SUBSTANCE NAME: | HEPARIN SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
ROUTE: | INTRAVENOUS; SUBCUTANEOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2011-06-08 |
END MARKETING DATE: | 0000-00-00 |
Heparin Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Heparin Sodium from Sandoz Inc |
LABELER NAME: | Sandoz Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5000([USP’U]/mL) |
START MARKETING DATE: | 2011-06-08 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0781-3327_6bfbbf70-320b-4f30-a80b-cbe3ca936dfd |
PRODUCT NDC: | 0781-3327 |
APPLICATION NUMBER: | ANDA091682 |
Other HEPARIN SODIUM Pharmaceutical Manufacturers / Labelers: