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
70771-1529-3	70771-1529	HUMAN PRESCRIPTION DRUG	doxepin	doxepin	TABLET	ORAL	20240630	N/A	ANDA	ANDA202761	Zydus Lifesciences Limited	DOXEPIN HYDROCHLORIDE	6 mg/1	30 TABLET in 1 BOTTLE (70771-1529-3)
70771-1529-4	70771-1529	HUMAN PRESCRIPTION DRUG	doxepin	doxepin	TABLET	ORAL	20240630	N/A	ANDA	ANDA202761	Zydus Lifesciences Limited	DOXEPIN HYDROCHLORIDE	6 mg/1	10 BLISTER PACK in 1 CARTON (70771-1529-4) / 10 TABLET in 1 BLISTER PACK
70771-1529-5	70771-1529	HUMAN PRESCRIPTION DRUG	doxepin	doxepin	TABLET	ORAL	20240630	N/A	ANDA	ANDA202761	Zydus Lifesciences Limited	DOXEPIN HYDROCHLORIDE	6 mg/1	500 TABLET in 1 BOTTLE (70771-1529-5)
70771-1529-9	70771-1529	HUMAN PRESCRIPTION DRUG	doxepin	doxepin	TABLET	ORAL	20240630	N/A	ANDA	ANDA202761	Zydus Lifesciences Limited	DOXEPIN HYDROCHLORIDE	6 mg/1	90 TABLET in 1 BOTTLE (70771-1529-9)