"69656-101-02" National Drug Code (NDC)

NDC Code	69656-101-02
Package Description	2 TABLET in 1 BLISTER PACK (69656-101-02)
Product NDC	69656-101
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Varubi
Non-Proprietary Name	Rolapitant
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20151007
End Marketing Date	20211031
Marketing Category Name	NDA
Application Number	NDA206500
Manufacturer	GlaxoSmithLine LLC
Substance Name	ROLAPITANT HYDROCHLORIDE
Strength	90
Strength Unit	mg/1
Pharmacy Classes	Neurokinin 1 Antagonists [MoA],Substance P/Neurokinin-1 Receptor Antagonist [EPC],Cytochrome P450 2D6 Inhibitors [MoA],Breast Cancer Resistance Protein Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]