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=ANDA211034"
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
43598-452-02 43598-452 HUMAN PRESCRIPTION DRUG Albendazole Albendazole TABLET, FILM COATED ORAL 20210126 N/A ANDA ANDA211034 Dr.Reddys Laboratories Inc ALBENDAZOLE 200 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (43598-452-02)
43598-452-17 43598-452 HUMAN PRESCRIPTION DRUG Albendazole Albendazole TABLET, FILM COATED ORAL 20210126 N/A ANDA ANDA211034 Dr.Reddys Laboratories Inc ALBENDAZOLE 200 mg/1 1 BLISTER PACK in 1 CARTON (43598-452-17) / 8 TABLET, FILM COATED in 1 BLISTER PACK
43598-452-63 43598-452 HUMAN PRESCRIPTION DRUG Albendazole Albendazole TABLET, FILM COATED ORAL 20210126 N/A ANDA ANDA211034 Dr.Reddys Laboratories Inc ALBENDAZOLE 200 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (43598-452-63)
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