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=ANDA089685"
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
70518-3108-0 70518-3108 HUMAN PRESCRIPTION DRUG Perphenazine Perphenazine TABLET, FILM COATED ORAL 20210528 20270321 ANDA ANDA089685 REMEDYREPACK INC. PERPHENAZINE 8 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3108-0)
0781-8046-01 0781-8046 HUMAN PRESCRIPTION DRUG Perphenazine Perphenazine TABLET, FILM COATED ORAL 20180828 20270321 ANDA ANDA089685 Sandoz Inc PERPHENAZINE 2 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-8046-01)
0781-8047-01 0781-8047 HUMAN PRESCRIPTION DRUG Perphenazine Perphenazine TABLET, FILM COATED ORAL 20180828 20270321 ANDA ANDA089685 Sandoz Inc PERPHENAZINE 4 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-8047-01)
0781-8048-01 0781-8048 HUMAN PRESCRIPTION DRUG Perphenazine Perphenazine TABLET, FILM COATED ORAL 20180828 20270321 ANDA ANDA089685 Sandoz Inc PERPHENAZINE 8 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-8048-01)
0781-8049-01 0781-8049 HUMAN PRESCRIPTION DRUG Perphenazine Perphenazine TABLET, FILM COATED ORAL 20180828 20270321 ANDA ANDA089685 Sandoz Inc PERPHENAZINE 16 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-8049-01)
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