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
68788-7811-3	68788-7811	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20201103	N/A	ANDA	ANDA040230	Preferred Pharmaceuticals Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (68788-7811-3)
68788-7811-6	68788-7811	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20201103	N/A	ANDA	ANDA040230	Preferred Pharmaceuticals Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	60 TABLET in 1 BOTTLE (68788-7811-6)
67296-1039-7	67296-1039	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	19990226	N/A	ANDA	ANDA040230	RedPharm Drug, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	15 TABLET in 1 BOTTLE (67296-1039-7)
67296-1039-9	67296-1039	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	19990226	N/A	ANDA	ANDA040230	RedPharm Drug, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	56 TABLET in 1 BOTTLE (67296-1039-9)
71610-209-09	71610-209	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20181218	N/A	ANDA	ANDA040230	Aphena Pharma Solutions - Tennessee, LLC	DICYCLOMINE HYDROCHLORIDE	20 mg/1	9000 TABLET in 1 BOTTLE (71610-209-09)
70518-0755-1	70518-0755	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20190130	N/A	ANDA	ANDA040230	REMEDYREPACK INC.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	180 TABLET in 1 BOTTLE, PLASTIC (70518-0755-1)
67296-1039-1	67296-1039	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	19990226	N/A	ANDA	ANDA040230	RedPharm Drug, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	10 TABLET in 1 BOTTLE (67296-1039-1)