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=ANDA075964"
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
71205-303-30 71205-303 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20190801 N/A ANDA ANDA075964 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BOTTLE (71205-303-30)
71205-303-78 71205-303 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20190801 N/A ANDA ANDA075964 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET in 1 BOTTLE (71205-303-78)
71205-303-90 71205-303 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20190801 N/A ANDA ANDA075964 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET in 1 BOTTLE (71205-303-90)
71205-303-60 71205-303 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20190801 N/A ANDA ANDA075964 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET in 1 BOTTLE (71205-303-60)
71205-303-72 71205-303 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20190801 N/A ANDA ANDA075964 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET in 1 BOTTLE (71205-303-72)
71205-303-40 71205-303 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20190801 N/A ANDA ANDA075964 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET in 1 BOTTLE (71205-303-40)
67296-1021-2 67296-1021 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20210101 N/A ANDA ANDA075964 RedPharm Drug, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET in 1 BOTTLE (67296-1021-2)
67296-1021-5 67296-1021 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20020622 N/A ANDA ANDA075964 RedPharm Drug, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET in 1 BOTTLE (67296-1021-5)
67296-1021-6 67296-1021 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20020622 N/A ANDA ANDA075964 RedPharm Drug, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 6 TABLET in 1 BOTTLE (67296-1021-6)
67296-1021-7 67296-1021 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20210101 N/A ANDA ANDA075964 RedPharm Drug, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET in 1 BOTTLE (67296-1021-7)
67296-1021-3 67296-1021 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20020622 N/A ANDA ANDA075964 RedPharm Drug, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BOTTLE (67296-1021-3)
67296-1021-1 67296-1021 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20020622 N/A ANDA ANDA075964 RedPharm Drug, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 10 TABLET in 1 BOTTLE (67296-1021-1)
67296-1021-4 67296-1021 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20020622 N/A ANDA ANDA075964 RedPharm Drug, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 45 TABLET in 1 BOTTLE (67296-1021-4)
58118-0377-8 58118-0377 HUMAN PRESCRIPTION DRUG tramadol hydrochloride tramadol hydrochloride TABLET ORAL 20200526 N/A ANDA ANDA075964 Clinical Solutions Wholesale, LLC TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET in 1 BLISTER PACK (58118-0377-8)
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