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 DescriptionAnticoagulant Sodium Citrate from Medsep Corporation
LABELER NAME: Medsep Corporation
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Haemonetics Manufacturing IncSodium Citrate
Medsep CorporationAnticoagulant Sodium Citrate