FDA approval for Allopurinol - Zyloprim clinical trails
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FDA Approval for Allopurinol - Zyloprim

The generic Allopurinol is the bioequivalent to the registered branded medicine Zyloprim developed and produced by the world renowned pharmaceutical manufacturers named Prometheus Laboratories Inc., of the United States. The medicine in tablets form Zyloprim–Allopurinol has been granted approval by the Food and Drugs Administration–FDA under abbreviated New Drug Application-aNDA. The drug has been indicated in the treatment of the patients having signs and symptoms of primary or secondary phase of gout disorders, treating the patients having leukemia, lymphoma and malignancies and are undergoing chemotherapy for cancer which causes increase of serum and urinary uric acid levels, treating the patients having persistent calcium oxalate calculi whose routine uric acid secretion are increased.

The pharmacology and usage of Allopurinol – Zyloprim denotes that the structural analog of the natural purine base hypoxanthine drug is used for preventing gout and renal calculi occurring due to either uric acid or calcium oxalate and for treating uric acid nephropathy, hyperuricemia associated with primary or secondary gout as well as certain solid malignancies or tumors. The mechanism of this drug is that it reduces or lowers the enzyme xanthine oxidase, preventing the adaptation of the oxypurine hypoxanthine and xanthine to uric acid. The drug is also proved of helping the assimilation of hypoxanthine and xanthine into DNA and RNA thereby helping further reduction of serum uric acid concentrations. Based on the positive findings of the clinical trials on the Allopurinol – Zyloprim drug it is approved for manufacture, sale and distribute in the United States in various dose strengths in tablet forms.
 

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