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=ANDA211571"
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
43598-069-42 43598-069 HUMAN OTC DRUG Esomeprazole Magnesium Esomeprazole Magnesium TABLET, DELAYED RELEASE ORAL 20231230 N/A ANDA ANDA211571 Dr. Reddys Laboratories Inc ESOMEPRAZOLE MAGNESIUM 20 mg/1 3 BOTTLE in 1 CARTON (43598-069-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
75907-119-27 75907-119 HUMAN OTC DRUG Esomeprazole Magnesium Esomeprazole Magnesium TABLET, DELAYED RELEASE ORAL 20231230 N/A ANDA ANDA211571 Dr. Reddys Laboratories Inc ESOMEPRAZOLE MAGNESIUM 20 mg/1 2 BOTTLE in 1 CARTON (75907-119-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
75907-119-33 75907-119 HUMAN OTC DRUG Esomeprazole Magnesium Esomeprazole Magnesium TABLET, DELAYED RELEASE ORAL 20231230 N/A ANDA ANDA211571 Dr. Reddys Laboratories Inc ESOMEPRAZOLE MAGNESIUM 20 mg/1 3 BOTTLE in 1 CARTON (75907-119-33) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
75907-119-52 75907-119 HUMAN OTC DRUG Esomeprazole Magnesium Esomeprazole Magnesium TABLET, DELAYED RELEASE ORAL 20231230 N/A ANDA ANDA211571 Dr. Reddys Laboratories Inc ESOMEPRAZOLE MAGNESIUM 20 mg/1 1 BOTTLE in 1 CARTON (75907-119-52) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase