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
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)
70518-3822-6 70518-3822 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20231103 N/A ANDA ANDA212517 REMEDYREPACK INC. NAPROXEN 500 mg/1 28 TABLET in 1 BOTTLE, PLASTIC (70518-3822-6)
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)
68788-7946-1 68788-7946 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210628 N/A ANDA ANDA212517 Preferred Pharmaceuticals, Inc. NAPROXEN 375 mg/1 100 TABLET in 1 BOTTLE (68788-7946-1)
68788-7946-2 68788-7946 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210628 N/A ANDA ANDA212517 Preferred Pharmaceuticals, Inc. NAPROXEN 375 mg/1 20 TABLET in 1 BOTTLE (68788-7946-2)
68788-7946-3 68788-7946 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210628 N/A ANDA ANDA212517 Preferred Pharmaceuticals, Inc. NAPROXEN 375 mg/1 30 TABLET in 1 BOTTLE (68788-7946-3)
68788-7946-6 68788-7946 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210628 N/A ANDA ANDA212517 Preferred Pharmaceuticals, Inc. NAPROXEN 375 mg/1 60 TABLET in 1 BOTTLE (68788-7946-6)
68788-7946-8 68788-7946 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210628 N/A ANDA ANDA212517 Preferred Pharmaceuticals, Inc. NAPROXEN 375 mg/1 120 TABLET in 1 BOTTLE (68788-7946-8)
68788-7946-9 68788-7946 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210628 N/A ANDA ANDA212517 Preferred Pharmaceuticals, Inc. NAPROXEN 375 mg/1 90 TABLET in 1 BOTTLE (68788-7946-9)
71205-597-10 71205-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210806 N/A ANDA ANDA212517 Proficient Rx LP NAPROXEN 500 mg/1 10 TABLET in 1 BOTTLE (71205-597-10)
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)
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)
71205-597-30 71205-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20210804 N/A ANDA ANDA212517 Proficient Rx LP NAPROXEN 500 mg/1 30 TABLET in 1 BOTTLE (71205-597-30)
71205-597-40 71205-597 HUMAN PRESCRIPTION DRUG Naproxen Naproxen TABLET ORAL 20211124 N/A ANDA ANDA212517 Proficient Rx LP NAPROXEN 500 mg/1 40 TABLET in 1 BOTTLE (71205-597-40)
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