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=ANDA078329"
符合检索条件的记录共 142 条，共 8 页，当前第 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
69238-1101-5 69238-1101 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20140401 N/A ANDA ANDA078329 Amneal Pharmaceuticals NY LLC IBUPROFEN 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69238-1101-5)
71610-890-80 71610-890 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250321 N/A ANDA ANDA078329 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-890-80)
71610-895-80 71610-895 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250401 N/A ANDA ANDA078329 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-895-80)
71610-895-92 71610-895 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250401 N/A ANDA ANDA078329 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71610-895-92)
71610-895-60 71610-895 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250401 N/A ANDA ANDA078329 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-895-60)
71610-890-60 71610-890 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250321 N/A ANDA ANDA078329 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-890-60)
71610-895-70 71610-895 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250401 N/A ANDA ANDA078329 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71610-895-70)
72789-185-20 72789-185 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210706 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-185-20)
72789-185-90 72789-185 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210518 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-185-90)
72789-186-30 72789-186 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210518 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-30)
72789-186-60 72789-186 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210518 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-60)
72789-186-82 72789-186 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210511 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-82)
72789-186-90 72789-186 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210518 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-90)
72789-187-30 72789-187 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210518 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-30)
72789-187-60 72789-187 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20200821 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-60)
72789-187-82 72789-187 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210518 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-82)
72789-187-90 72789-187 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210518 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-187-90)
72789-200-10 72789-200 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210928 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-10)
72789-200-12 72789-200 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20211011 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-12)
72789-200-15 72789-200 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20210921 N/A ANDA ANDA078329 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-200-15)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase