美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
0078-0709-94	0078-0709	HUMAN PRESCRIPTION DRUG	TABRECTA	capmatinib	TABLET, FILM COATED	ORAL	20200506	N/A	NDA	NDA213591	Novartis Pharmaceuticals Corporation	CAPMATINIB HYDROCHLORIDE	150 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (0078-0709-94)
0078-0716-56	0078-0716	HUMAN PRESCRIPTION DRUG	TABRECTA	capmatinib	TABLET, FILM COATED	ORAL	20200506	N/A	NDA	NDA213591	Novartis Pharmaceuticals Corporation	CAPMATINIB HYDROCHLORIDE	200 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (0078-0716-56)
0078-0716-94	0078-0716	HUMAN PRESCRIPTION DRUG	TABRECTA	capmatinib	TABLET, FILM COATED	ORAL	20200506	N/A	NDA	NDA213591	Novartis Pharmaceuticals Corporation	CAPMATINIB HYDROCHLORIDE	200 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (0078-0716-94)
0078-0709-56	0078-0709	HUMAN PRESCRIPTION DRUG	TABRECTA	capmatinib	TABLET, FILM COATED	ORAL	20200506	N/A	NDA	NDA213591	Novartis Pharmaceuticals Corporation	CAPMATINIB HYDROCHLORIDE	150 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (0078-0709-56)