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Drug Product Composition: Rolapitant hydrochloride

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USFDA APPLICATION NUMBER - 208399 / DOSAGE - EMULSION;INTRAVENOUS - EQ 166.5MG BASE/92.5ML (EQ 1.8MG BASE/ML)

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