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=ANDA208416"
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
43598-468-38 43598-468 HUMAN PRESCRIPTION DRUG Abiraterone Acetate Abiraterone Acetate TABLET ORAL 20230911 N/A ANDA ANDA208416 Dr. Reddys Laboratories Inc ABIRATERONE ACETATE 500 mg/1 6 BLISTER PACK in 1 CARTON (43598-468-38) / 10 TABLET in 1 BLISTER PACK (43598-468-79)
43598-468-60 43598-468 HUMAN PRESCRIPTION DRUG Abiraterone Acetate Abiraterone Acetate TABLET ORAL 20230911 N/A ANDA ANDA208416 Dr. Reddys Laboratories Inc ABIRATERONE ACETATE 500 mg/1 60 TABLET in 1 BOTTLE (43598-468-60)
43598-358-31 43598-358 HUMAN PRESCRIPTION DRUG Abiraterone Acetate Abiraterone Acetate TABLET ORAL 20211220 N/A ANDA ANDA208416 Dr. Reddys Laboratories Inc ABIRATERONE ACETATE 250 mg/1 3 BLISTER PACK in 1 CARTON (43598-358-31) / 10 TABLET in 1 BLISTER PACK (43598-358-79)
43598-358-04 43598-358 HUMAN PRESCRIPTION DRUG Abiraterone Acetate Abiraterone Acetate TABLET ORAL 20200519 N/A ANDA ANDA208416 Dr. Reddys Laboratories Inc ABIRATERONE ACETATE 250 mg/1 120 TABLET in 1 BOTTLE (43598-358-04)
16714-963-01 16714-963 HUMAN PRESCRIPTION DRUG Abiraterone Acetate Abiraterone Acetate TABLET ORAL 20200519 N/A ANDA ANDA208416 NorthStar Rx LLC ABIRATERONE ACETATE 250 mg/1 120 TABLET in 1 BOTTLE (16714-963-01)
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