Heparin Sodium (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Heparin Sodium drug offered from Fresenius Kabi USA, LLC. 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: | Fresenius Kabi USA, LLC |
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, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2010-06-18 |
END MARKETING DATE: | 0000-00-00 |
Heparin Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Heparin Sodium from Fresenius Kabi USA, LLC |
LABELER NAME: | Fresenius Kabi USA, LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5000([USP’U]/mL) |
START MARKETING DATE: | 2010-06-18 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-047_3bbce5c9-3dd0-4675-9a87-a2d786b435e6 |
PRODUCT NDC: | 63323-047 |
APPLICATION NUMBER: | NDA017651 |
Other HEPARIN SODIUM Pharmaceutical Manufacturers / Labelers: