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USFDA APPLICATION NUMBER - 19909 / DOSAGE - SUSPENSION;ORAL - 200MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 | 200mg in 5 |
Inactive Ingredients
| Ingredient Name | Mylan Pharmaceuticals Inc. | Renaissance Pharma, Inc. |
|---|---|---|
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM(K679OBS311) | ||
| GLYCERIN(PDC6A3C0OX) | ||
| METHYLPARABEN(A2I8C7HI9T) | ||
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||
| PROPYLPARABEN(Z8IX2SC1OH) | ||
| SORBITOL(506T60A25R) |
