FDA Drug Approval, N020363, FAMVIR

FDA Drug Approval, N020363, FAMVIR

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NDA: 020363
Company: NOVARTIS
Drug Name: FAMVIR
Active Ingredients: FAMCICLOVIR
Strength: 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: TABLET;ORAL
Action Date: 06/29/1994
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity

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