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=ANDA075682"
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
71205-604-15 71205-604 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210927 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 400 mg/1 15 TABLET in 1 BOTTLE (71205-604-15)
71205-604-20 71205-604 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210927 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 400 mg/1 20 TABLET in 1 BOTTLE (71205-604-20)
71205-604-21 71205-604 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210927 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 400 mg/1 21 TABLET in 1 BOTTLE (71205-604-21)
71205-604-30 71205-604 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210827 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 400 mg/1 30 TABLET in 1 BOTTLE (71205-604-30)
71205-604-40 71205-604 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210927 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 400 mg/1 40 TABLET in 1 BOTTLE (71205-604-40)
71205-604-60 71205-604 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210827 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 400 mg/1 60 TABLET in 1 BOTTLE (71205-604-60)
71205-604-90 71205-604 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20210827 N/A ANDA ANDA075682 Proficient Rx LP IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (71205-604-90)
55111-682-01 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 100 TABLET in 1 BOTTLE (55111-682-01)
55111-682-05 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 500 TABLET in 1 BOTTLE (55111-682-05)
55111-682-09 55111-682 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 400 mg/1 90 TABLET in 1 BOTTLE (55111-682-09)
55111-683-01 55111-683 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 600 mg/1 100 TABLET in 1 BOTTLE (55111-683-01)
55111-683-05 55111-683 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 600 mg/1 500 TABLET in 1 BOTTLE (55111-683-05)
55111-683-09 55111-683 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 600 mg/1 90 TABLET in 1 BOTTLE (55111-683-09)
55111-683-30 55111-683 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 600 mg/1 30 TABLET in 1 BOTTLE (55111-683-30)
55111-683-50 55111-683 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 600 mg/1 50 TABLET in 1 BOTTLE (55111-683-50)
55111-684-01 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 100 TABLET in 1 BOTTLE (55111-684-01)
55111-684-05 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 500 TABLET in 1 BOTTLE (55111-684-05)
55111-684-09 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 90 TABLET in 1 BOTTLE (55111-684-09)
55111-684-30 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 30 TABLET in 1 BOTTLE (55111-684-30)
55111-684-50 55111-684 HUMAN PRESCRIPTION DRUG IBU Ibuprofen TABLET ORAL 20081120 N/A ANDA ANDA075682 Dr. Reddy's Laboratories Limited IBUPROFEN 800 mg/1 50 TABLET in 1 BOTTLE (55111-684-50)
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