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=ANDA213699"
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
27241-203-60 27241-203 HUMAN PRESCRIPTION DRUG Naproxen and esomeprazole magnesium Naproxen and esomeprazole magnesium TABLET, DELAYED RELEASE ORAL 20221006 N/A ANDA ANDA213699 Ajanta Pharma USA Inc. ESOMEPRAZOLE MAGNESIUM; NAPROXEN 20 mg/1; 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (27241-203-60)
68788-8766-6 68788-8766 HUMAN PRESCRIPTION DRUG Naproxen and esomeprazole magnesium Naproxen and esomeprazole magnesium TABLET, DELAYED RELEASE ORAL 20241108 N/A ANDA ANDA213699 Preferred Pharmaceuticals Inc. ESOMEPRAZOLE MAGNESIUM TRIHYDRATE; NAPROXEN 20 mg/1; 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8766-6)
68788-8766-3 68788-8766 HUMAN PRESCRIPTION DRUG Naproxen and esomeprazole magnesium Naproxen and esomeprazole magnesium TABLET, DELAYED RELEASE ORAL 20241108 N/A ANDA ANDA213699 Preferred Pharmaceuticals Inc. ESOMEPRAZOLE MAGNESIUM TRIHYDRATE; NAPROXEN 20 mg/1; 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8766-3)
27241-202-60 27241-202 HUMAN PRESCRIPTION DRUG Naproxen and esomeprazole magnesium Naproxen and esomeprazole magnesium TABLET, DELAYED RELEASE ORAL 20221006 N/A ANDA ANDA213699 Ajanta Pharma USA Inc. ESOMEPRAZOLE MAGNESIUM; NAPROXEN 20 mg/1; 375 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (27241-202-60)
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