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INDIA'S RANBAXY GETS USFDA APPROVAL FOR GANCICLOVAR DRUG.

AsiaPulse News

| July 01, 2003 | COPYRIGHT 2003 Asia Pulse Pty Ltd. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

NEW DELHI, July 1 Asia Pulse - Ranbaxy Laboratories (BSE:RANB) said Monday it has received US Food and Drug Administration approval to manufacture and market Ganciclovir capsules in 250 mg and 500mg strength, generic version of Roche's Cytovene.

Ganciclovir capsules are indicated for the prevention of Cytomegalovirus (CMV) disease in solid organ transplant recipients and in individuals with advanced HIV infection at risk for devloping CMV ...

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Source: HighBeam Research, INDIA'S RANBAXY GETS USFDA APPROVAL FOR GANCICLOVAR DRUG.

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