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
80425-0276-6 80425-0276 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230217 N/A ANDA ANDA208708 Advanced Rx Pharmacy of Tennessee, LLC TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, COATED in 1 BOTTLE (80425-0276-6)
80425-0276-7 80425-0276 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230331 N/A ANDA ANDA208708 Advanced Rx Pharmacy of Tennessee, LLC TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, COATED in 1 BOTTLE (80425-0276-7)
80425-0276-8 80425-0276 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230331 N/A ANDA ANDA208708 Advanced Rx Pharmacy of Tennessee, LLC TRAMADOL HYDROCHLORIDE 50 mg/1 240 TABLET, COATED in 1 BOTTLE (80425-0276-8)
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)
68788-8121-9 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 90 TABLET, COATED in 1 BOTTLE (68788-8121-9)
71335-2721-1 71335-2721 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250926 N/A ANDA ANDA208708 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 50 mg/1 8 TABLET, COATED in 1 BOTTLE (71335-2721-1)
71335-2721-2 71335-2721 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250926 N/A ANDA ANDA208708 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 50 mg/1 84 TABLET, COATED in 1 BOTTLE (71335-2721-2)
71335-2721-3 71335-2721 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250926 N/A ANDA ANDA208708 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 50 mg/1 56 TABLET, COATED in 1 BOTTLE (71335-2721-3)
71335-2721-4 71335-2721 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250926 N/A ANDA ANDA208708 Bryant Ranch Prepack TRAMADOL HYDROCHLORIDE 50 mg/1 10 TABLET, COATED in 1 BOTTLE (71335-2721-4)
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)
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)
67296-1834-3 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)
67296-1834-4 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)
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