"50242-175-07" National Drug Code (NDC)

NDC Code	50242-175-07
Package Description	1 BOTTLE, GLASS in 1 CARTON (50242-175-07) / 80 mL in 1 BOTTLE, GLASS
Product NDC	50242-175
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Evrysdi
Non-Proprietary Name	Risdiplam
Dosage Form	POWDER, FOR SOLUTION
Usage	ORAL
Start Marketing Date	20200807
Marketing Category Name	NDA
Application Number	NDA213535
Manufacturer	Genentech Inc.
Substance Name	RISDIPLAM
Strength	.75
Strength Unit	mg/mL
Pharmacy Classes	Increased Protein Synthesis [PE], Multidrug and Toxin Extrusion Transporter 1 Inhibitors [MoA], Multidrug and Toxin Extrusion Transporter 2 K Inhibitors [MoA], Survival of Motor Neuron 2 Splicing Modifier [EPC], Survival of Motor Neuron 2 Splicing Modifiers [MoA]