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
82982-029-60	82982-029	HUMAN PRESCRIPTION DRUG	Dicyclomine	Dicyclomine hydrochloride	TABLET	ORAL	20230314	N/A	ANDA	ANDA040161	Pharmasource Meds, LLC	DICYCLOMINE HYDROCHLORIDE	20 mg/1	60 TABLET in 1 BOTTLE (82982-029-60)
0143-1227-01	0143-1227	HUMAN PRESCRIPTION DRUG	Dicyclomine	Dicyclomine hydrochloride	TABLET	ORAL	19961001	N/A	ANDA	ANDA040161	Hikma Pharmaceuticals USA Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0143-1227-01)
0143-1227-10	0143-1227	HUMAN PRESCRIPTION DRUG	Dicyclomine	Dicyclomine hydrochloride	TABLET	ORAL	19961001	N/A	ANDA	ANDA040161	Hikma Pharmaceuticals USA Inc.	DICYCLOMINE HYDROCHLORIDE	20 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0143-1227-10)