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)
检索条件:" 注册申请号=ANDA084363"
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
0591-5335-01 0591-5335 HUMAN PRESCRIPTION DRUG Trihexyphenidyl Hydrochloride Trihexyphenidyl Hydrochloride TABLET ORAL 19871101 N/A ANDA ANDA084363 Actavis Pharma, Inc. TRIHEXYPHENIDYL HYDROCHLORIDE 2 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (0591-5335-01)
0591-5335-10 0591-5335 HUMAN PRESCRIPTION DRUG Trihexyphenidyl Hydrochloride Trihexyphenidyl Hydrochloride TABLET ORAL 19871101 N/A ANDA ANDA084363 Actavis Pharma, Inc. TRIHEXYPHENIDYL HYDROCHLORIDE 2 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5335-10)
70518-1612-1 70518-1612 HUMAN PRESCRIPTION DRUG Trihexyphenidyl Hydrochloride Trihexyphenidyl Hydrochloride TABLET ORAL 20191223 N/A ANDA ANDA084363 REMEDYREPACK INC. TRIHEXYPHENIDYL HYDROCHLORIDE 2 mg/1 100 POUCH in 1 BOX (70518-1612-1) / 1 TABLET in 1 POUCH (70518-1612-2)
70518-1021-0 70518-1021 HUMAN PRESCRIPTION DRUG Trihexyphenidyl Hydrochloride Trihexyphenidyl Hydrochloride TABLET ORAL 20180216 N/A ANDA ANDA084363 REMEDYREPACK INC. TRIHEXYPHENIDYL HYDROCHLORIDE 2 mg/1 30 TABLET in 1 BLISTER PACK (70518-1021-0)
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