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GeneraMedix Inc. receives FDA approval for Fluorouracil Injection, USP

On April 26, 2007 GeneraMedix Inc. received approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Applications (ANDAs) for Fluorouracil Injection, USP. GeneraMedix will market Fluorouracil 50 mg/mL in 10 mL, 20 mL, 50 mL and 100 mL vials. The product is AP rated and equivalent to the reference listed drugs of Abraxis Pharmaceutical Products and Sicor Pharmaceuticals, Inc.

For product information please contact:

GeneraMedix Inc. Customer Service
1-866–GENERA–1
(1-866-436-3721)

 
   
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