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=ANDA212517"
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
63629-8513-1 63629-8513 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20200301 N/A ANDA ANDA212517 Bryant Ranch Prepack NAPROXEN 375 mg/1 100 TABLET in 1 BOTTLE (63629-8513-1)
63629-8514-1 63629-8514 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20200301 N/A ANDA ANDA212517 Bryant Ranch Prepack NAPROXEN 500 mg/1 500 TABLET in 1 BOTTLE (63629-8514-1)
63629-8515-1 63629-8515 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20200301 N/A ANDA ANDA212517 Bryant Ranch Prepack NAPROXEN 500 mg/1 100 TABLET in 1 BOTTLE (63629-8515-1)
70518-3822-0 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20230806 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 30 TABLET in 1 BLISTER PACK (70518-3822-0)
70518-3822-1 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20230823 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (70518-3822-1)
70518-3822-2 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20230823 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (70518-3822-2)
70518-3822-3 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20230824 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (70518-3822-3)
70518-3822-4 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20230824 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (70518-3822-4)
70518-3822-5 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20230909 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 6 TABLET in 1 BLISTER PACK (70518-3822-5)
70518-3822-7 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20240223 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 12 TABLET in 1 BOTTLE, PLASTIC (70518-3822-7)
71610-591-53 71610-591 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210809 N/A ANDA ANDA212517 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 375 mg/1 60 TABLET in 1 BOTTLE (71610-591-53)
71610-591-80 71610-591 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210809 N/A ANDA ANDA212517 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 375 mg/1 180 TABLET in 1 BOTTLE (71610-591-80)
71610-592-53 71610-592 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210809 N/A ANDA ANDA212517 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 250 mg/1 60 TABLET in 1 BOTTLE (71610-592-53)
71610-592-80 71610-592 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210809 N/A ANDA ANDA212517 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 250 mg/1 180 TABLET in 1 BOTTLE (71610-592-80)
71610-597-53 71610-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20211026 N/A ANDA ANDA212517 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 500 mg/1 60 TABLET in 1 BOTTLE (71610-597-53)
71610-597-70 71610-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210909 N/A ANDA ANDA212517 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 500 mg/1 120 TABLET in 1 BOTTLE (71610-597-70)
71610-597-80 71610-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20211026 N/A ANDA ANDA212517 Aphena Pharma Solutions - Tennessee, LLC NAPROXEN 500 mg/1 180 TABLET in 1 BOTTLE (71610-597-80)
50090-5645-0 50090-5645 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210913 N/A ANDA ANDA212517 A-S Medication Solutions NAPROXEN 500 mg/1 15 TABLET in 1 BOTTLE (50090-5645-0)
50090-5645-1 50090-5645 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210913 N/A ANDA ANDA212517 A-S Medication Solutions NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE (50090-5645-1)
50090-5645-2 50090-5645 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210913 N/A ANDA ANDA212517 A-S Medication Solutions NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (50090-5645-2)
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