Heparin Sodium (Sagent Pharmaceuticals)
Welcome to the PulseAid listing for the Heparin Sodium drug offered from Sagent Pharmaceuticals. 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: | Sagent Pharmaceuticals |
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: | ANDA |
START MARKETING DATE: | 2010-07-06 |
END MARKETING DATE: | 0000-00-00 |
Heparin Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Heparin Sodium from Sagent Pharmaceuticals |
LABELER NAME: | Sagent Pharmaceuticals |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1000([USP’U]/mL) |
START MARKETING DATE: | 2010-07-06 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 25021-400_5e78e6b5-8d1c-47c1-aab1-e2fb4eb92ecb |
PRODUCT NDC: | 25021-400 |
APPLICATION NUMBER: | ANDA090808 |
Other HEPARIN SODIUM Pharmaceutical Manufacturers / Labelers: