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
73473-902-01	73473-902	HUMAN PRESCRIPTION DRUG	DICYCLOMINE HYDROCHLORIDE	DICYCLOMINE HYDROCHLORIDE	TABLET	ORAL	20250610	N/A	ANDA	ANDA216760	Solaris Pharma Corporation	DICYCLOMINE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (73473-902-01)
73473-902-10	73473-902	HUMAN PRESCRIPTION DRUG	DICYCLOMINE HYDROCHLORIDE	DICYCLOMINE HYDROCHLORIDE	TABLET	ORAL	20250610	N/A	ANDA	ANDA216760	Solaris Pharma Corporation	DICYCLOMINE HYDROCHLORIDE	20 mg/1	1000 TABLET in 1 BOTTLE (73473-902-10)
0832-6052-10	0832-6052	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20230209	20260630	ANDA	ANDA216760	Upsher-Smith Laboratories, LLC	DICYCLOMINE HYDROCHLORIDE	20 mg/1	1000 TABLET in 1 BOTTLE (0832-6052-10)
0832-6052-11	0832-6052	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20230209	20260930	ANDA	ANDA216760	Upsher-Smith Laboratories, LLC	DICYCLOMINE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (0832-6052-11)
67296-1891-3	67296-1891	HUMAN PRESCRIPTION DRUG	Dicyclomine hydrochloride	Dicyclomine hydrochloride	TABLET	ORAL	20230209	N/A	ANDA	ANDA216760	RedPharm Drug, Inc	DICYCLOMINE HYDROCHLORIDE	20 mg/1	15 TABLET in 1 BOTTLE (67296-1891-3)