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=NDA020547"
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
49884-554-02 49884-554 HUMAN PRESCRIPTION DRUG Zafirlukast zafirlukast TABLET, COATED ORAL 20101119 20240930 NDA NDA020547 Par Pharmaceutical, Inc. ZAFIRLUKAST 20 mg/1 60 TABLET, COATED in 1 BOTTLE (49884-554-02)
64380-187-01 64380-187 HUMAN PRESCRIPTION DRUG Zafirlukast zafirlukast TABLET, COATED ORAL 20220915 N/A NDA NDA020547 Strides Pharma Science Limited ZAFIRLUKAST 10 mg/1 60 TABLET, COATED in 1 BOTTLE (64380-187-01)
64380-188-01 64380-188 HUMAN PRESCRIPTION DRUG Zafirlukast zafirlukast TABLET, COATED ORAL 20220801 N/A NDA NDA020547 Strides Pharma Science Limited ZAFIRLUKAST 20 mg/1 60 TABLET, COATED in 1 BOTTLE (64380-188-01)
42291-970-60 42291-970 HUMAN PRESCRIPTION DRUG Zafirlukast zafirlukast TABLET, COATED ORAL 20230405 N/A NDA NDA020547 AvKARE ZAFIRLUKAST 10 mg/1 60 TABLET, COATED in 1 BOTTLE (42291-970-60)
42291-971-60 42291-971 HUMAN PRESCRIPTION DRUG Zafirlukast zafirlukast TABLET, COATED ORAL 20230405 N/A NDA NDA020547 AvKARE ZAFIRLUKAST 20 mg/1 60 TABLET, COATED in 1 BOTTLE (42291-971-60)
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