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
70771-1356-3	70771-1356	HUMAN PRESCRIPTION DRUG	Dutasteride and tamsulosin hydrochloride	Dutasteride and tamsulosin hydrochloride	CAPSULE	ORAL	20180604	N/A	ANDA	ANDA207769	Zydus Lifesciences Limited	DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE	.5 mg/1; .4 mg/1	30 CAPSULE in 1 BOTTLE (70771-1356-3)
70771-1356-9	70771-1356	HUMAN PRESCRIPTION DRUG	Dutasteride and tamsulosin hydrochloride	Dutasteride and tamsulosin hydrochloride	CAPSULE	ORAL	20180604	N/A	ANDA	ANDA207769	Zydus Lifesciences Limited	DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE	.5 mg/1; .4 mg/1	90 CAPSULE in 1 BOTTLE (70771-1356-9)
68382-640-06	68382-640	HUMAN PRESCRIPTION DRUG	Dutasteride and tamsulosin hydrochloride	Dutasteride and tamsulosin hydrochloride	CAPSULE	ORAL	20180604	N/A	ANDA	ANDA207769	Zydus Pharmaceuticals USA Inc.	DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE	.5 mg/1; .4 mg/1	30 CAPSULE in 1 BOTTLE (68382-640-06)
68382-640-16	68382-640	HUMAN PRESCRIPTION DRUG	Dutasteride and tamsulosin hydrochloride	Dutasteride and tamsulosin hydrochloride	CAPSULE	ORAL	20180604	N/A	ANDA	ANDA207769	Zydus Pharmaceuticals USA Inc.	DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE	.5 mg/1; .4 mg/1	90 CAPSULE in 1 BOTTLE (68382-640-16)