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
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)
71205-597-14 71205-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210826 N/A ANDA ANDA212517 Proficient Rx LP NAPROXEN 500 mg/1 14 TABLET in 1 BOTTLE (71205-597-14)
71205-597-15 71205-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20221107 N/A ANDA ANDA212517 Proficient Rx LP NAPROXEN 500 mg/1 15 TABLET in 1 BOTTLE (71205-597-15)
50090-7676-0 50090-7676 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20251008 N/A ANDA ANDA212517 A-S Medication Solutions NAPROXEN 500 mg/1 90 TABLET in 1 BOTTLE (50090-7676-0)
82804-229-30 82804-229 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250724 N/A ANDA ANDA212517 Proficient Rx LP NAPROXEN 250 mg/1 30 TABLET in 1 BOTTLE (82804-229-30)
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)
80425-0175-2 80425-0175 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20200301 N/A ANDA ANDA212517 Advanced Rx Pharmacy of Tennessee, LLC NAPROXEN 375 mg/1 60 TABLET in 1 BOTTLE (80425-0175-2)
71205-597-20 71205-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210920 N/A ANDA ANDA212517 Proficient Rx LP NAPROXEN 500 mg/1 20 TABLET in 1 BOTTLE (71205-597-20)
70518-3486-0 70518-3486 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20230823 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 375 mg/1 30 TABLET in 1 BLISTER PACK (70518-3486-0)
70518-3486-1 70518-3486 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20250701 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 375 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (70518-3486-1)
85509-1436-9 85509-1436 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20251114 N/A ANDA ANDA212517 PHOENIX RX LLC NAPROXEN 500 mg/1 90 TABLET in 1 BOTTLE (85509-1436-9)
85509-1436-3 85509-1436 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20251114 N/A ANDA ANDA212517 PHOENIX RX LLC NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (85509-1436-3)
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