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=ANDA211825"
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
70518-4055-0 70518-4055 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20240419 N/A ANDA ANDA211825 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 50 mg/1 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4055-0)
50090-5789-0 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5789-0)
50090-5789-1 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-5789-1)
50090-5789-2 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (50090-5789-2)
50090-5789-3 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-5789-3)
50090-5789-4 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (50090-5789-4)
50090-5789-5 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-5789-5)
50090-5789-9 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (50090-5789-9)
50090-5790-1 50090-5790 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20220208 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5790-1)
50090-5790-2 50090-5790 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-5790-2)
50090-5790-3 50090-5790 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20220629 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-5790-3)
29300-355-10 29300-355 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20191104 N/A ANDA ANDA211825 Unichem Pharmaceuticals (USA), Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-355-10)
29300-355-05 29300-355 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20191104 N/A ANDA ANDA211825 Unichem Pharmaceuticals (USA), Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-355-05)
29300-355-01 29300-355 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20191104 N/A ANDA ANDA211825 Unichem Pharmaceuticals (USA), Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-355-01)
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