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
51079-375-20	51079-375	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide Hydrochloride	Chlordiazepoxide Hydrochloride	CAPSULE	ORAL	20220526	N/A	ANDA	ANDA083116	Mylan Institutional Inc.	CHLORDIAZEPOXIDE HYDROCHLORIDE	10 mg/1	100 BLISTER PACK in 1 CARTON (51079-375-20) / 1 CAPSULE in 1 BLISTER PACK (51079-375-01)
70518-1752-1	70518-1752	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide Hydrochloride	Chlordiazepoxide Hydrochloride	CAPSULE	ORAL	20211210	N/A	ANDA	ANDA083116	REMEDYREPACK INC.	CHLORDIAZEPOXIDE HYDROCHLORIDE	10 mg/1	30 CAPSULE in 1 BLISTER PACK (70518-1752-1)
0555-0033-02	0555-0033	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide Hydrochloride	Chlordiazepoxide Hydrochloride	CAPSULE	ORAL	19900930	N/A	ANDA	ANDA083116	Teva Pharmaceuticals USA, Inc.	CHLORDIAZEPOXIDE HYDROCHLORIDE	10 mg/1	100 CAPSULE in 1 BOTTLE (0555-0033-02)
0555-0033-05	0555-0033	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide Hydrochloride	Chlordiazepoxide Hydrochloride	CAPSULE	ORAL	19900930	N/A	ANDA	ANDA083116	Teva Pharmaceuticals USA, Inc.	CHLORDIAZEPOXIDE HYDROCHLORIDE	10 mg/1	1000 CAPSULE in 1 BOTTLE (0555-0033-05)
58118-1033-8	58118-1033	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide Hydrochloride	Chlordiazepoxide Hydrochloride	CAPSULE	ORAL	20190219	N/A	ANDA	ANDA083116	Clinical Solutions Wholesale, LLC	CHLORDIAZEPOXIDE HYDROCHLORIDE	10 mg/1	30 CAPSULE in 1 BLISTER PACK (58118-1033-8)