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
82804-142-72 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20241105 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, COATED in 1 BOTTLE (82804-142-72)
82804-142-78 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250115 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, COATED in 1 BOTTLE (82804-142-78)
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)
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)
72888-080-05 72888-080 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230724 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 50 mg/1 500 TABLET, COATED in 1 BOTTLE (72888-080-05)
76420-733-00 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 1000 TABLET, COATED in 1 BOTTLE (76420-733-00)
76420-733-01 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, COATED in 1 BOTTLE (76420-733-01)
76420-733-02 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250814 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 2 TABLET, COATED in 1 BOTTLE (76420-733-02)
76420-733-05 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-733-05)
76420-733-10 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250814 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 1 TABLET, COATED in 1 BOTTLE (76420-733-10)
76420-733-12 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250714 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, COATED in 1 BOTTLE (76420-733-12)
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)
72888-163-00 72888-163 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230724 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 75 mg/1 1000 TABLET, COATED in 1 BOTTLE (72888-163-00)
72888-163-01 72888-163 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230724 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 75 mg/1 100 TABLET, COATED in 1 BOTTLE (72888-163-01)
72888-163-05 72888-163 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230724 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 75 mg/1 500 TABLET, COATED in 1 BOTTLE (72888-163-05)
72888-163-30 72888-163 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230724 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 75 mg/1 30 TABLET, COATED in 1 BOTTLE (72888-163-30)
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)
52817-195-00 52817-195 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200901 N/A ANDA ANDA208708 TRUPHARMA LLC TRAMADOL HYDROCHLORIDE 50 mg/1 1000 TABLET, COATED in 1 BOTTLE (52817-195-00)
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