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=ANDA208708"
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
67296-1834-4 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, COATED in 1 BOTTLE (67296-1834-4)
67296-1834-6 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 6 TABLET, COATED in 1 BOTTLE (67296-1834-6)
67296-1834-7 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, COATED in 1 BOTTLE (67296-1834-7)
67296-1917-7 67296-1917 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200224 N/A ANDA ANDA208708 RedPharm Drug TRAMADOL HYDROCHLORIDE 100 mg/1 15 TABLET, COATED in 1 BOTTLE (67296-1917-7)
67296-1834-3 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (67296-1834-3)
67296-1834-2 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, COATED in 1 BOTTLE (67296-1834-2)
67296-1834-1 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 10 TABLET, COATED in 1 BOTTLE (67296-1834-1)
82804-142-15 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20241021 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, COATED in 1 BOTTLE (82804-142-15)
82804-142-90 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, COATED in 1 BOTTLE (82804-142-90)
82804-142-20 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, COATED in 1 BOTTLE (82804-142-20)
82804-142-30 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (82804-142-30)
82804-142-60 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, COATED in 1 BOTTLE (82804-142-60)
76420-733-30 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (76420-733-30)
76420-733-60 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-733-60)
76420-733-90 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, COATED in 1 BOTTLE (76420-733-90)
76420-734-00 76420-734 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 1000 TABLET, COATED in 1 BOTTLE (76420-734-00)
76420-734-01 76420-734 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 100 TABLET, COATED in 1 BOTTLE (76420-734-01)
76420-734-05 76420-734 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-734-05)
76420-734-30 76420-734 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, COATED in 1 BOTTLE (76420-734-30)
76420-734-60 76420-734 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-734-60)
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