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=ANDA209794"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
71209-063-02 71209-063 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20171229 N/A ANDA ANDA209794 Cadila Pharmaceuticals Limited METRONIDAZOLE 500 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71209-063-02)
71209-063-10 71209-063 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20171229 N/A ANDA ANDA209794 Cadila Pharmaceuticals Limited METRONIDAZOLE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71209-063-10)
71209-062-02 71209-062 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20171229 N/A ANDA ANDA209794 Cadila Pharmaceuticals Limited METRONIDAZOLE 250 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71209-062-02)
71209-062-10 71209-062 HUMAN PRESCRIPTION DRUG Metronidazole Metronidazole TABLET, FILM COATED ORAL 20171229 N/A ANDA ANDA209794 Cadila Pharmaceuticals Limited METRONIDAZOLE 250 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (71209-062-10)
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