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
61919-376-14 61919-376 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20190822 N/A ANDA ANDA078250 Direct_Rx NAPROXEN 500 mg/1 14 TABLET in 1 BOTTLE (61919-376-14)
61919-376-28 61919-376 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20190822 N/A ANDA ANDA078250 Direct_Rx NAPROXEN 500 mg/1 28 TABLET in 1 BOTTLE (61919-376-28)
61919-376-30 61919-376 HUMAN PRESCRIPTION DRUG NAPROXEN NAPROXEN TABLET ORAL 20190822 N/A ANDA ANDA078250 Direct_Rx NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (61919-376-30)
68071-2245-6 68071-2245 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20200824 N/A ANDA ANDA078250 NuCare Pharmaceuticals,Inc. NAPROXEN 500 mg/1 6 TABLET in 1 BOTTLE (68071-2245-6)
80425-0050-1 80425-0050 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Advanced Rx Pharmacy of Tennessee, LLC NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE (80425-0050-1)
80425-0050-2 80425-0050 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20070701 N/A ANDA ANDA078250 Advanced Rx Pharmacy of Tennessee, LLC NAPROXEN 500 mg/1 90 TABLET in 1 BOTTLE (80425-0050-2)
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