Citra Anticoagulants Announces FDA Approval for NO CLOT-50, ACD-A
Citra Anticoagulants Announces FDA Approval to Market NO CLOT-50 Anticoagulant Citrate Dextrose Solution, Solution A, ACD-A
Braintree, MA (PRWEB) November 23, 2004 -- Citra Anticoagulants, Inc. announces its parent company, Cytosol Laboratories, Inc., has received U.S. Food and Drug Administration (FDA) approval for NO CLOT-50 Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P., commonly known as ACD-A, for use in the extracorporeal blood processing with Autologous Platelet Rich Plasma (PRP) Systems in the production of platelet rich plasma. NO CLOT-50 is the anticoagulant of choice to prevent clotting of the whole blood during the extracorporeal blood processing with Autologous PRP Systems.
NO CLOT-50 is a United States Pharmacopeia formulated product containing 50 milliliters of ACD-A. NO CLOT-50 prevents the coagulation of blood by virtue of its citrate ions ability to chelate the ionized calcium present in blood to form a non-ionized calcium-citrate complex. When the total dose of citrate ions is greater than the total amount of ionized calcium, blood clotting is prevented.
NO CLOT-50 is marketed and distributed exclusively by Citra Anticoagulants, Inc.
About Citra Anticoagulants
Headquartered in Braintree, Massachusetts, Citra Anticoagulants, Inc., is a wholly-owned subsidiary of Cytosol Laboratories, Inc., a privately held company, which develops and manufactures sterile, medical solutions. Citra Anticoagulants markets and distributes various citrate-based anticoagulants to a multitude of markets within the medical community.
Contact:
Citra Anticoagulants, Inc.
Ronald H. Lewis, Ph.D., President
rlewis@t3cc.com
Adrienne Summers, Team Customer
asummers@t3cc.com
781-848-2174
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