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"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
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
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
75907-119-27 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
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
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