"50242-202-01" National Drug Code (NDC)

NDC Code	50242-202-01
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (50242-202-01) / 30 TABLET in 1 BOTTLE, PLASTIC
Product NDC	50242-202
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Evrysdi
Non-Proprietary Name	Risdiplam
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20250211
Marketing Category Name	NDA
Application Number	NDA219285
Manufacturer	Genentech, Inc.
Substance Name	RISDIPLAM
Strength	5
Strength Unit	mg/1
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]