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=ANDA078250"
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
60760-190-20 60760-190 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20171110 N/A ANDA ANDA078250 St. Mary's Medical Park Pharmacy NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (60760-190-20)
60760-190-30 60760-190 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20171110 N/A ANDA ANDA078250 St. Mary's Medical Park Pharmacy NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (60760-190-30)
60760-190-60 60760-190 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20171110 N/A ANDA ANDA078250 St. Mary's Medical Park Pharmacy NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (60760-190-60)
68788-8844-1 68788-8844 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250320 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 375 mg/1 100 TABLET in 1 BOTTLE (68788-8844-1)
68788-8844-2 68788-8844 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250320 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 375 mg/1 20 TABLET in 1 BOTTLE (68788-8844-2)
68788-8844-3 68788-8844 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250320 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 375 mg/1 30 TABLET in 1 BOTTLE (68788-8844-3)
68788-8844-6 68788-8844 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250320 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 375 mg/1 60 TABLET in 1 BOTTLE (68788-8844-6)
68788-8844-8 68788-8844 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250320 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 375 mg/1 120 TABLET in 1 BOTTLE (68788-8844-8)
68788-8844-9 68788-8844 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250320 N/A ANDA ANDA078250 Preferred Pharmaceuticals Inc. NAPROXEN 375 mg/1 90 TABLET in 1 BOTTLE (68788-8844-9)
68462-188-01 68462-188 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 250 mg/1 100 TABLET in 1 BOTTLE (68462-188-01)
68462-188-05 68462-188 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 250 mg/1 500 TABLET in 1 BOTTLE (68462-188-05)
68462-189-01 68462-189 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 375 mg/1 100 TABLET in 1 BOTTLE (68462-189-01)
68462-189-05 68462-189 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Glenmark Pharmaceuticals Inc., USA NAPROXEN 375 mg/1 500 TABLET in 1 BOTTLE (68462-189-05)
63187-028-10 63187-028 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20190301 N/A ANDA ANDA078250 Proficient Rx LP NAPROXEN 500 mg/1 10 TABLET in 1 BOTTLE (63187-028-10)
63187-028-14 63187-028 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20170501 N/A ANDA ANDA078250 Proficient Rx LP NAPROXEN 500 mg/1 14 TABLET in 1 BOTTLE (63187-028-14)
63187-028-15 63187-028 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20140501 N/A ANDA ANDA078250 Proficient Rx LP NAPROXEN 500 mg/1 15 TABLET in 1 BOTTLE (63187-028-15)
63187-028-20 63187-028 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20140501 N/A ANDA ANDA078250 Proficient Rx LP NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE (63187-028-20)
63187-028-30 63187-028 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20140501 N/A ANDA ANDA078250 Proficient Rx LP NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (63187-028-30)
63187-028-40 63187-028 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20170601 N/A ANDA ANDA078250 Proficient Rx LP NAPROXEN 500 mg/1 40 TABLET in 1 BOTTLE (63187-028-40)
63187-028-45 63187-028 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20140501 N/A ANDA ANDA078250 Proficient Rx LP NAPROXEN 500 mg/1 45 TABLET in 1 BOTTLE (63187-028-45)
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