"71274-170-60" National Drug Code (NDC)

NDC Code	71274-170-60
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (71274-170-60) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC	71274-170
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Joenja
Non-Proprietary Name	Leniolisib
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20230329
Marketing Category Name	NDA
Application Number	NDA217759
Manufacturer	Pharming Healthcare Inc.
Substance Name	LENIOLISIB PHOSPHATE
Strength	70
Strength Unit	mg/1
Pharmacy Classes	Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 1A2 Inhibitors [MoA], Kinase Inhibitor [EPC], Organic Anion Transporting Polypeptide 1B1 Inhibitors [MoA], Organic Anion Transporting Polypeptide 1B3 Inhibitors [MoA], Phosphoinositide 3-Kinase delta Inhibitors [MoA]