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"
符合检索条件的记录共 117 条，共 6 页，当前第 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
52817-196-10 52817-196 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200224 N/A ANDA ANDA208708 TRUPHARMA LLC TRAMADOL HYDROCHLORIDE 100 mg/1 100 TABLET, COATED in 1 BOTTLE (52817-196-10)
52817-196-50 52817-196 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200224 N/A ANDA ANDA208708 TRUPHARMA LLC TRAMADOL HYDROCHLORIDE 100 mg/1 500 TABLET, COATED in 1 BOTTLE (52817-196-50)
76420-732-00 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 1000 TABLET, COATED in 1 BOTTLE (76420-732-00)
76420-732-01 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 100 TABLET, COATED in 1 BOTTLE (76420-732-01)
76420-732-05 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-732-05)
76420-732-30 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 30 TABLET, COATED in 1 BOTTLE (76420-732-30)
76420-732-60 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-732-60)
76420-732-90 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 90 TABLET, COATED in 1 BOTTLE (76420-732-90)
68788-8121-1 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, COATED in 1 BOTTLE (68788-8121-1)
68788-8121-2 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, COATED in 1 BOTTLE (68788-8121-2)
68788-8121-3 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (68788-8121-3)
68788-8121-4 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, COATED in 1 BOTTLE (68788-8121-4)
68788-8121-5 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, COATED in 1 BOTTLE (68788-8121-5)
68788-8121-6 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, COATED in 1 BOTTLE (68788-8121-6)
68788-8121-7 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 50 TABLET, COATED in 1 BOTTLE (68788-8121-7)
68788-8121-8 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, COATED in 1 BOTTLE (68788-8121-8)
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)
82804-142-20 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)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase