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=ANDA076003"
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
63187-063-78 63187-063 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20140501 N/A ANDA ANDA076003 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, COATED in 1 BOTTLE (63187-063-78)
63187-063-90 63187-063 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20140501 N/A ANDA ANDA076003 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, COATED in 1 BOTTLE (63187-063-90)
63187-063-20 63187-063 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20161101 N/A ANDA ANDA076003 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, COATED in 1 BOTTLE (63187-063-20)
63187-063-30 63187-063 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20140501 N/A ANDA ANDA076003 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (63187-063-30)
63187-063-40 63187-063 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20140501 N/A ANDA ANDA076003 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, COATED in 1 BOTTLE (63187-063-40)
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