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
0069-2299-30	0069-2299	HUMAN PRESCRIPTION DRUG	Vizimpro	dacomitinib	TABLET, FILM COATED	ORAL	20181004	N/A	NDA	NDA211288	Pfizer Laboratories Div Pfizer Inc	DACOMITINIB	45 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-2299-30)
0069-1198-30	0069-1198	HUMAN PRESCRIPTION DRUG	Vizimpro	dacomitinib	TABLET, FILM COATED	ORAL	20181004	N/A	NDA	NDA211288	Pfizer Laboratories Div Pfizer Inc	DACOMITINIB	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-1198-30)
0069-0197-30	0069-0197	HUMAN PRESCRIPTION DRUG	Vizimpro	dacomitinib	TABLET, FILM COATED	ORAL	20181004	N/A	NDA	NDA211288	Pfizer Laboratories Div Pfizer Inc	DACOMITINIB	15 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-0197-30)
63539-197-90	63539-197	HUMAN PRESCRIPTION DRUG	Vizimpro	dacomitinib	TABLET, FILM COATED	ORAL	20190201	N/A	NDA	NDA211288	U.S. Pharmaceuticals	DACOMITINIB	15 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63539-197-90)