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
67184-0531-1	67184-0531	HUMAN PRESCRIPTION DRUG	Gefitinib	Gefitinib	TABLET, COATED	ORAL	20230213	N/A	ANDA	ANDA211591	Qilu Pharmaceutical Co., Ltd.	GEFITINIB	250 mg/1	30 TABLET, COATED in 1 BOTTLE (67184-0531-1)
67184-0531-2	67184-0531	HUMAN PRESCRIPTION DRUG	Gefitinib	Gefitinib	TABLET, COATED	ORAL	20230213	N/A	ANDA	ANDA211591	Qilu Pharmaceutical Co., Ltd.	GEFITINIB	250 mg/1	500 TABLET, COATED in 1 BOTTLE (67184-0531-2)
67184-0531-3	67184-0531	HUMAN PRESCRIPTION DRUG	Gefitinib	Gefitinib	TABLET, COATED	ORAL	20230213	N/A	ANDA	ANDA211591	Qilu Pharmaceutical Co., Ltd.	GEFITINIB	250 mg/1	3 BLISTER PACK in 1 CARTON (67184-0531-3) / 10 TABLET, COATED in 1 BLISTER PACK
50742-366-30	50742-366	HUMAN PRESCRIPTION DRUG	Gefitinib	Gefitinib	TABLET, COATED	ORAL	20230427	N/A	ANDA	ANDA211591	Ingenus Pharmaceuticals, LLC	GEFITINIB	250 mg/1	30 TABLET, COATED in 1 BOTTLE (50742-366-30)