Heparin Sodium (Hospira, Inc.)
Welcome to the PulseAid listing for the Heparin Sodium drug offered from Hospira, 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: | Hospira, 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 |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2005-03-31 |
END MARKETING DATE: | 0000-00-00 |
Heparin Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Heparin Sodium from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200([USP’U]/100mL) |
START MARKETING DATE: | 2005-03-31 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-7620_e588f69a-85db-46fe-afc8-ad0010f18774 |
PRODUCT NDC: | 0409-7620 |
APPLICATION NUMBER: | NDA018916 |
Other HEPARIN SODIUM Pharmaceutical Manufacturers / Labelers: