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=ANDA078352"
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
50090-6724-0 50090-6724 HUMAN PRESCRIPTION DRUG DESLORATADINE DESLORATADINE TABLET, FILM COATED ORAL 20231005 N/A ANDA ANDA078352 A-S Medication Solutions DESLORATADINE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6724-0)
68180-153-02 68180-153 HUMAN PRESCRIPTION DRUG DESLORATADINE DESLORATADINE TABLET, FILM COATED ORAL 20130225 N/A ANDA ANDA078352 Lupin Pharmaceuticals, Inc. DESLORATADINE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68180-153-02)
68180-153-01 68180-153 HUMAN PRESCRIPTION DRUG DESLORATADINE DESLORATADINE TABLET, FILM COATED ORAL 20130225 N/A ANDA ANDA078352 Lupin Pharmaceuticals, Inc. DESLORATADINE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68180-153-01)
71335-1000-1 71335-1000 HUMAN PRESCRIPTION DRUG DESLORATADINE DESLORATADINE TABLET, FILM COATED ORAL 20181113 N/A ANDA ANDA078352 Bryant Ranch Prepack DESLORATADINE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1000-1)
71335-1000-2 71335-1000 HUMAN PRESCRIPTION DRUG DESLORATADINE DESLORATADINE TABLET, FILM COATED ORAL 20240409 N/A ANDA ANDA078352 Bryant Ranch Prepack DESLORATADINE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1000-2)
50090-4794-1 50090-4794 HUMAN PRESCRIPTION DRUG DESLORATADINE DESLORATADINE TABLET, FILM COATED ORAL 20191212 N/A ANDA ANDA078352 A-S Medication Solutions DESLORATADINE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-4794-1)
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