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filingDate 2007-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f31656c8a45814bf5646196f9322d9dd
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publicationDate 2008-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PE-20081578-A1
titleOfInvention VALGANCICLOVIR POWDER FORMULATION
abstract IT REFERS TO A SOLID PHARMACEUTICAL DOSAGE FORM FOR ORAL ADMINISTRATION, AFTER BEING CONSTITUTED IN WATER, CONSISTING OF: (a) AN EFFECTIVE THERAPEUTIC AMOUNT OF VALGANCICLOVIR HYDROCHLORIDE PRESENT IN AN AMOUNT OF 10% TO 90% PESTIO. ; AND (b) A NON-HYGROSCOPIC ORGANIC ACID PRESENT IN A SUFFICIENT AMOUNT TO STABILIZE VANGANCICLOVIR HYDROCHLORIDE IN A PREDETERMINED AMOUNT OF WATER, AND ALSO LOWER THE pH OF THE CONSTITUTE SOLUTION, TO A SELECTED pH OF 3.8 ACID OR LESS, IF THE pH IS SET TO ACIDED 3.8 SUCCINICO AND AC. ADIPICO. IT ALSO REFERS TO A LIQUID DOSAGE FORM. SUCH FORMULATION IS USEFUL IN THE TREATMENT OR CONTROL OF HERPES SIMPLEX VIRUSES AND CYTOMEGALOVIRUS
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