
USFDA APPLICATION NUMBER - 206500 / DOSAGE - TABLET;ORAL - EQ 90MG BASE
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| ROLAPITANT HYDROCHLORIDE(UNII: 57O5S1QSAQ) (rolapitant - UNII:NLE429IZUC) | rolapitant | 90mg |
| rolapitant(UNII: NLE429IZUC) (rolapitant - UNII:NLE429IZUC) | rolapitant | 1.8mg in 1 |
Inactive Ingredients