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
68180-423-08	68180-423	HUMAN PRESCRIPTION DRUG	CEFIXIME	CEFIXIME	CAPSULE	ORAL	20201014	N/A	NDA AUTHORIZED GENERIC	NDA203195	Lupin Pharmaceuticals, Inc.	CEFIXIME	400 mg/1	50 CAPSULE in 1 BOTTLE (68180-423-08)
68180-423-11	68180-423	HUMAN PRESCRIPTION DRUG	CEFIXIME	CEFIXIME	CAPSULE	ORAL	20201014	N/A	NDA AUTHORIZED GENERIC	NDA203195	Lupin Pharmaceuticals, Inc.	CEFIXIME	400 mg/1	1 BLISTER PACK in 1 CARTON (68180-423-11) / 10 CAPSULE in 1 BLISTER PACK
70518-3221-2	70518-3221	HUMAN PRESCRIPTION DRUG	CEFIXIME	CEFIXIME	CAPSULE	ORAL	20211104	N/A	NDA AUTHORIZED GENERIC	NDA203195	REMEDYREPACK INC.	CEFIXIME	400 mg/1	2 POUCH in 1 BOX (70518-3221-2) / 1 CAPSULE in 1 POUCH (70518-3221-3)
70518-3221-4	70518-3221	HUMAN PRESCRIPTION DRUG	CEFIXIME	CEFIXIME	CAPSULE	ORAL	20220302	N/A	NDA AUTHORIZED GENERIC	NDA203195	REMEDYREPACK INC.	CEFIXIME	400 mg/1	2 CAPSULE in 1 BOTTLE, PLASTIC (70518-3221-4)