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=ANDA091416"
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
71335-0973-1 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 30 TABLET in 1 BOTTLE (71335-0973-1)
71335-0973-2 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 60 TABLET in 1 BOTTLE (71335-0973-2)
71335-0973-3 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 20 TABLET in 1 BOTTLE (71335-0973-3)
71335-0973-4 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 120 TABLET in 1 BOTTLE (71335-0973-4)
71335-0973-5 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 10 TABLET in 1 BOTTLE (71335-0973-5)
71335-0973-6 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 90 TABLET in 1 BOTTLE (71335-0973-6)
71335-0973-7 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 40 TABLET in 1 BOTTLE (71335-0973-7)
71335-0973-8 71335-0973 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20181023 N/A ANDA ANDA091416 Bryant Ranch Prepack NAPROXEN 250 mg/1 45 TABLET in 1 BOTTLE (71335-0973-8)
25000-140-14 25000-140 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20110228 N/A ANDA ANDA091416 MARKSANS PHARMA LIMITED NAPROXEN 500 mg/1 1000 TABLET in 1 BOTTLE (25000-140-14)
25000-140-19 25000-140 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20110228 N/A ANDA ANDA091416 MARKSANS PHARMA LIMITED NAPROXEN 500 mg/1 4 BAG in 1 BOX (25000-140-19) / 3500 TABLET in 1 BAG
72189-136-14 72189-136 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20201015 N/A ANDA ANDA091416 DIRECT RX NAPROXEN 500 mg/1 14 TABLET in 1 BOTTLE (72189-136-14)
72189-136-20 72189-136 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20201015 N/A ANDA ANDA091416 DIRECT RX NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE (72189-136-20)
72189-136-30 72189-136 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20201015 N/A ANDA ANDA091416 DIRECT RX NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (72189-136-30)
72189-136-60 72189-136 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20201015 N/A ANDA ANDA091416 DIRECT RX NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE (72189-136-60)
72189-136-71 72189-136 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20201015 N/A ANDA ANDA091416 DIRECT RX NAPROXEN 500 mg/1 100 TABLET in 1 BOTTLE (72189-136-71)
72189-136-90 72189-136 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20201015 N/A ANDA ANDA091416 DIRECT RX NAPROXEN 500 mg/1 90 TABLET in 1 BOTTLE (72189-136-90)
71610-436-53 71610-436 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200616 N/A ANDA ANDA091416 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (71610-436-53)
71610-436-60 71610-436 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20210331 N/A ANDA ANDA091416 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 500 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71610-436-60)
71610-436-80 71610-436 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20200616 N/A ANDA ANDA091416 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 500 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (71610-436-80)
42708-140-20 42708-140 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20210423 N/A ANDA ANDA091416 QPharma Inc NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (42708-140-20)
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