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
70518-1586-1	70518-1586	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20191021	N/A	ANDA	ANDA077562	REMEDYREPACK INC.	ZIPRASIDONE HYDROCHLORIDE	20 mg/1	30 POUCH in 1 BOX (70518-1586-1) / 1 CAPSULE in 1 POUCH (70518-1586-2)
0781-2166-60	0781-2166	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20130213	N/A	ANDA	ANDA077562	Sandoz Inc	ZIPRASIDONE HYDROCHLORIDE	40 mg/1	60 CAPSULE in 1 BOTTLE (0781-2166-60)
70518-2367-2	70518-2367	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20240627	N/A	ANDA	ANDA077562	REMEDYREPACK INC.	ZIPRASIDONE HYDROCHLORIDE	40 mg/1	30 CAPSULE in 1 BLISTER PACK (70518-2367-2)
0781-2167-60	0781-2167	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20130213	N/A	ANDA	ANDA077562	Sandoz Inc	ZIPRASIDONE HYDROCHLORIDE	60 mg/1	60 CAPSULE in 1 BOTTLE (0781-2167-60)
0781-2168-60	0781-2168	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20130213	N/A	ANDA	ANDA077562	Sandoz Inc	ZIPRASIDONE HYDROCHLORIDE	80 mg/1	60 CAPSULE in 1 BOTTLE (0781-2168-60)
0781-2164-60	0781-2164	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20130213	N/A	ANDA	ANDA077562	Sandoz Inc	ZIPRASIDONE HYDROCHLORIDE	20 mg/1	60 CAPSULE in 1 BOTTLE (0781-2164-60)
63187-168-30	63187-168	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20190101	N/A	ANDA	ANDA077562	Proficient Rx LP	ZIPRASIDONE HYDROCHLORIDE	20 mg/1	30 CAPSULE in 1 BOTTLE (63187-168-30)
63187-168-60	63187-168	HUMAN PRESCRIPTION DRUG	ziprasidone hydrochloride	ziprasidone hydrochloride	CAPSULE	ORAL	20190101	N/A	ANDA	ANDA077562	Proficient Rx LP	ZIPRASIDONE HYDROCHLORIDE	20 mg/1	60 CAPSULE in 1 BOTTLE (63187-168-60)