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
70518-1657-1	70518-1657	HUMAN PRESCRIPTION DRUG	Trihexyphenidyl Hydrochloride	Trihexyphenidyl Hydrochloride	TABLET	ORAL	20190123	N/A	ANDA	ANDA084364	REMEDYREPACK INC.	TRIHEXYPHENIDYL HYDROCHLORIDE	5 mg/1	100 POUCH in 1 BOX (70518-1657-1) / 1 TABLET in 1 POUCH (70518-1657-2)
70518-1140-0	70518-1140	HUMAN PRESCRIPTION DRUG	Trihexyphenidyl Hydrochloride	Trihexyphenidyl Hydrochloride	TABLET	ORAL	20180426	N/A	ANDA	ANDA084364	REMEDYREPACK INC.	TRIHEXYPHENIDYL HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BLISTER PACK (70518-1140-0)
0591-5337-10	0591-5337	HUMAN PRESCRIPTION DRUG	Trihexyphenidyl Hydrochloride	Trihexyphenidyl Hydrochloride	TABLET	ORAL	19871101	N/A	ANDA	ANDA084364	Actavis Pharma, Inc.	TRIHEXYPHENIDYL HYDROCHLORIDE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (0591-5337-10)
0591-5337-01	0591-5337	HUMAN PRESCRIPTION DRUG	Trihexyphenidyl Hydrochloride	Trihexyphenidyl Hydrochloride	TABLET	ORAL	19871101	N/A	ANDA	ANDA084364	Actavis Pharma, Inc.	TRIHEXYPHENIDYL HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (0591-5337-01)