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
63020-180-30	63020-180	HUMAN PRESCRIPTION DRUG	Alunbrig	brigatinib	TABLET, FILM COATED	ORAL	20171002	N/A	NDA	NDA208772	Takeda Pharmaceuticals America, Inc.	BRIGATINIB	180 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63020-180-30)
63020-198-30	63020-198	HUMAN PRESCRIPTION DRUG	Alunbrig	brigatinib	KIT		20171002	N/A	NDA	NDA208772	Takeda Pharmaceuticals America, Inc.			1 KIT in 1 CARTON (63020-198-30) * 7 TABLET, FILM COATED in 1 BOTTLE (63020-090-07) * 23 TABLET, FILM COATED in 1 BOTTLE (63020-180-23)
63020-113-30	63020-113	HUMAN PRESCRIPTION DRUG	Alunbrig	brigatinib	TABLET, FILM COATED	ORAL	20171002	N/A	NDA	NDA208772	Takeda Pharmaceuticals America, Inc.	BRIGATINIB	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63020-113-30)
63020-090-30	63020-090	HUMAN PRESCRIPTION DRUG	Alunbrig	brigatinib	TABLET, FILM COATED	ORAL	20171002	N/A	NDA	NDA208772	Takeda Pharmaceuticals America, Inc.	BRIGATINIB	90 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63020-090-30)
63020-090-07	63020-090	HUMAN PRESCRIPTION DRUG	Alunbrig	brigatinib	TABLET, FILM COATED	ORAL	20171002	N/A	NDA	NDA208772	Takeda Pharmaceuticals America, Inc.	BRIGATINIB	90 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (63020-090-07)