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Drug Product Composition: Rolapitant hydrochloride

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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)
rolapitant90mg
rolapitant(UNII: NLE429IZUC)
(rolapitant - UNII:NLE429IZUC)
rolapitant1.8mg in 1

Inactive Ingredients