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
53002-3451-4	53002-3451	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20221231	N/A	ANDA	ANDA040230	RPK Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	40 TABLET in 1 BOTTLE (53002-3451-4)
53002-3451-1	53002-3451	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20221231	N/A	ANDA	ANDA040230	RPK Pharmaceuticals, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	10 TABLET in 1 BOTTLE (53002-3451-1)
0527-1282-01	0527-1282	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	19990226	N/A	ANDA	ANDA040230	Lannett Company, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (0527-1282-01)
0527-1282-05	0527-1282	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	19990226	N/A	ANDA	ANDA040230	Lannett Company, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	500 TABLET in 1 BOTTLE (0527-1282-05)
0527-1282-10	0527-1282	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	19990226	N/A	ANDA	ANDA040230	Lannett Company, Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	1000 TABLET in 1 BOTTLE (0527-1282-10)
72162-1077-9	72162-1077	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20230508	N/A	ANDA	ANDA040230	Bryant Ranch Prepack	DICYCLOMINE HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE (72162-1077-9)
72162-1077-3	72162-1077	HUMAN PRESCRIPTION DRUG	Dicyclomine Hydrochloride	Dicyclomine Hydrochloride	TABLET	ORAL	20230508	N/A	ANDA	ANDA040230	Bryant Ranch Prepack	DICYCLOMINE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (72162-1077-3)