USFDA APPLICATION NUMBER - 20363 / DOSAGE - TABLET;ORAL - 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
FAMCICLOVIR(UNII: QIC03ANI02) (PENCICLOVIR - UNII:359HUE8FJC) | FAMCICLOVIR | 500mg | 250mg | 125mg |
Inactive Ingredients
Ingredient Name | Novartis Pharmaceuticals Corporation |
---|---|
HYDROXYPROPYL CELLULOSE (TYPE H)(RFW2ET671P) | |
LACTOSE(J2B2A4N98G) | |
MAGNESIUM STEARATE(70097M6I30) | |
POLYETHYLENE GLYCOLS(3WJQ0SDW1A) | |
SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | |
TITANIUM DIOXIDE(15FIX9V2JP) |
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