"0078-0709-56" National Drug Code (NDC)

NDC Code	0078-0709-56
Package Description	56 TABLET, FILM COATED in 1 BOTTLE (0078-0709-56)
Product NDC	0078-0709
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tabrecta
Non-Proprietary Name	Capmatinib
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20200506
Marketing Category Name	NDA
Application Number	NDA213591
Manufacturer	Novartis Pharmaceuticals Corporation
Substance Name	CAPMATINIB HYDROCHLORIDE
Strength	150
Strength Unit	mg/1
Pharmacy Classes	Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 1A2 Inhibitors [MoA], Kinase Inhibitor [EPC], Mesenchymal Epithelial Transition Inhibitors [MoA], Multidrug and Toxin Extrusion Transporter 1 Inhibitors [MoA], Multidrug and Toxin Extrusion Transporter 2 K Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]