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=ANDA208511"
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
33342-307-10 33342-307 HUMAN PRESCRIPTION DRUG esomeprazole esomeprazole CAPSULE, DELAYED RELEASE ORAL 20241023 N/A ANDA ANDA208511 Macleods Pharmaceuticals Limited ESOMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-307-10)
33342-307-07 33342-307 HUMAN PRESCRIPTION DRUG esomeprazole esomeprazole CAPSULE, DELAYED RELEASE ORAL 20241023 N/A ANDA ANDA208511 Macleods Pharmaceuticals Limited ESOMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-307-07)
33342-306-10 33342-306 HUMAN PRESCRIPTION DRUG esomeprazole esomeprazole CAPSULE, DELAYED RELEASE ORAL 20241023 N/A ANDA ANDA208511 Macleods Pharmaceuticals Limited ESOMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-306-10)
33342-306-07 33342-306 HUMAN PRESCRIPTION DRUG esomeprazole esomeprazole CAPSULE, DELAYED RELEASE ORAL 20241023 N/A ANDA ANDA208511 Macleods Pharmaceuticals Limited ESOMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-306-07)
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