Anticoagulant Sodium Citrate (Medsep Corporation)
Welcome to the PulseAid listing for the Anticoagulant Sodium Citrate drug offered from Medsep Corporation. This Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] 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: | Medsep Corporation |
NON-PROPRIETARY NAME: | Sodium Citrate |
SUBSTANCE NAME: | SODIUM CITRATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2011-04-15 |
END MARKETING DATE: | 0000-00-00 |
Anticoagulant Sodium Citrate HUMAN PRESCRIPTION DRUG Details:
Item Description | Anticoagulant Sodium Citrate from Medsep Corporation |
LABELER NAME: | Medsep Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(g/250mL) |
START MARKETING DATE: | 2011-04-15 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62646-798_a083fb8e-3012-4d12-94d3-949a3188aba3 |
PRODUCT NDC: | 62646-798 |
APPLICATION NUMBER: | NDA760305 |
Other SODIUM CITRATE Pharmaceutical Manufacturers / Labelers: