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=ANDA206582"
符合检索条件的记录共 6 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
59726-737-14 59726-737 HUMAN OTC DRUG Omeprazole Omeprazole magnesium TABLET, DELAYED RELEASE ORAL 20200602 20251231 ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20.6 mg/1 1 BOTTLE in 1 CARTON (59726-737-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
59726-737-28 59726-737 HUMAN OTC DRUG Omeprazole Omeprazole magnesium TABLET, DELAYED RELEASE ORAL 20200602 20251231 ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20.6 mg/1 2 BOTTLE in 1 CARTON (59726-737-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
59726-737-42 59726-737 HUMAN OTC DRUG Omeprazole Omeprazole magnesium TABLET, DELAYED RELEASE ORAL 20200602 20251231 ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20.6 mg/1 3 BOTTLE in 1 CARTON (59726-737-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
59726-297-42 59726-297 HUMAN OTC DRUG Omeprazole Omeprazole magnesium TABLET, DELAYED RELEASE ORAL 20200602 20251231 ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20.6 mg/1 3 BOTTLE in 1 CARTON (59726-297-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
59726-297-28 59726-297 HUMAN OTC DRUG Omeprazole Omeprazole magnesium TABLET, DELAYED RELEASE ORAL 20200602 20251231 ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20.6 mg/1 2 BOTTLE in 1 CARTON (59726-297-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
59726-297-14 59726-297 HUMAN OTC DRUG Omeprazole Omeprazole magnesium TABLET, DELAYED RELEASE ORAL 20200602 20251231 ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20.6 mg/1 1 BOTTLE in 1 CARTON (59726-297-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
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