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USFDA APPLICATION NUMBER - 20089 / DOSAGE - TABLET;ORAL - 800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| ACYCLOVIR(UNII: X4HES1O11F) (ACYCLOVIR - UNII:X4HES1O11F) | ACYCLOVIR | 800mg |
Inactive Ingredients
| Ingredient Name | GlaxoSmithKline LLC | Prestium Pharma, Inc. |
|---|---|---|
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||
| FD&C BLUE NO. 2(L06K8R7DQK) | ||
| GELATIN, UNSPECIFIED(2G86QN327L) | ||
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | ||
| MAGNESIUM STEARATE(70097M6I30) | ||
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||
| POVIDONE, UNSPECIFIED(FZ989GH94E) | ||
| POVIDONES(FZ989GH94E) | ||
| SODIUM LAURYL SULFATE(368GB5141J) | ||
| SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | ||
| STARCH, CORN(O8232NY3SJ) | ||
| TITANIUM DIOXIDE(15FIX9V2JP) |
