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
68071-3255-9	68071-3255	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20170608	N/A	ANDA	ANDA085223	NuCare Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE (68071-3255-9)
67296-0126-0	67296-0126	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20120101	N/A	ANDA	ANDA085223	RedPharm Drug, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	28 TABLET in 1 BOTTLE (67296-0126-0)
67296-0126-1	67296-0126	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20120101	N/A	ANDA	ANDA085223	RedPharm Drug, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	10 TABLET in 1 BOTTLE (67296-0126-1)
67296-0126-5	67296-0126	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20120101	N/A	ANDA	ANDA085223	RedPharm Drug, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	56 TABLET in 1 BOTTLE (67296-0126-5)
67296-0126-7	67296-0126	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20120101	N/A	ANDA	ANDA085223	RedPharm Drug, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	15 TABLET in 1 BOTTLE (67296-0126-7)