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=ANDA208446"
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
0378-6921-91 0378-6921 HUMAN PRESCRIPTION DRUG Abiraterone Acetate abiraterone acetate TABLET, FILM COATED ORAL 20201214 N/A ANDA ANDA208446 Mylan Pharmaceuticals Inc. ABIRATERONE ACETATE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6921-91)
0378-6920-78 0378-6920 HUMAN PRESCRIPTION DRUG Abiraterone Acetate abiraterone acetate TABLET ORAL 20181121 N/A ANDA ANDA208446 Mylan Pharmaceuticals Inc. ABIRATERONE ACETATE 250 mg/1 120 TABLET in 1 BOTTLE, PLASTIC (0378-6920-78)
72162-2151-6 72162-2151 HUMAN PRESCRIPTION DRUG Abiraterone Acetate abiraterone acetate TABLET, FILM COATED ORAL 20231207 N/A ANDA ANDA208446 Bryant Ranch Prepack ABIRATERONE ACETATE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2151-6)
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