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=ANDA078003"
符合检索条件的记录共 3 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
61919-243-30 61919-243 HUMAN PRESCRIPTION DRUG ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM CAPSULE, DELAYED RELEASE ORAL 20210224 N/A ANDA ANDA078003 DIRECT RX ESOMEPRAZOLE MAGNESIUM DIHYDRATE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (61919-243-30)
0093-6451-98 0093-6451 HUMAN PRESCRIPTION DRUG Esomeprazole Magnesium Esomeprazole Magnesium CAPSULE, DELAYED RELEASE ORAL 20150217 20250131 ANDA ANDA078003 Teva Pharmaceuticals USA, Inc. ESOMEPRAZOLE MAGNESIUM DIHYDRATE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-6451-98)
0093-6451-56 0093-6451 HUMAN PRESCRIPTION DRUG Esomeprazole Magnesium Esomeprazole Magnesium CAPSULE, DELAYED RELEASE ORAL 20150217 20250131 ANDA ANDA078003 Teva Pharmaceuticals USA, Inc. ESOMEPRAZOLE MAGNESIUM DIHYDRATE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-6451-56)
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