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=ANDA211724"
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
70756-816-22 70756-816 HUMAN PRESCRIPTION DRUG Capecitabine Capecitabine TABLET, FILM COATED ORAL 20200901 N/A ANDA ANDA211724 Lifestar Pharma LLC CAPECITABINE 500 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70756-816-22)
62135-783-60 62135-783 HUMAN PRESCRIPTION DRUG Capecitabine Capecitabine TABLET ORAL 20231016 N/A ANDA ANDA211724 Chartwell RX, LLC CAPECITABINE 150 mg/1 60 TABLET in 1 BOTTLE (62135-783-60)
62135-784-12 62135-784 HUMAN PRESCRIPTION DRUG Capecitabine Capecitabine TABLET ORAL 20231016 N/A ANDA ANDA211724 Chartwell RX, LLC CAPECITABINE 500 mg/1 120 TABLET in 1 BOTTLE (62135-784-12)
70756-815-60 70756-815 HUMAN PRESCRIPTION DRUG Capecitabine Capecitabine TABLET, FILM COATED ORAL 20200901 N/A ANDA ANDA211724 Lifestar Pharma LLC CAPECITABINE 150 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70756-815-60)
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