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 115 条，共 6 页，当前第 4 页 ，可点击列名称排序
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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
70518-3824-3 70518-3824 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230818 N/A ANDA ANDA208708 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-3)
70518-3824-4 70518-3824 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230831 N/A ANDA ANDA208708 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-4)
70518-3824-5 70518-3824 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20231011 N/A ANDA ANDA208708 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-5)
70518-3824-6 70518-3824 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20251218 N/A ANDA ANDA208708 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-6)
72888-008-00 72888-008 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200224 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 100 mg/1 1000 TABLET, COATED in 1 BOTTLE (72888-008-00)
72888-008-01 72888-008 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200224 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 100 mg/1 100 TABLET, COATED in 1 BOTTLE (72888-008-01)
72888-008-05 72888-008 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200224 N/A ANDA ANDA208708 Advagen Pharma Limited TRAMADOL HYDROCHLORIDE 100 mg/1 500 TABLET, COATED in 1 BOTTLE (72888-008-05)
72189-311-12 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 12 TABLET, COATED in 1 BOTTLE (72189-311-12)
72189-311-20 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, COATED in 1 BOTTLE (72189-311-20)
72189-311-30 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (72189-311-30)
72189-311-40 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, COATED in 1 BOTTLE (72189-311-40)
72189-311-60 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, COATED in 1 BOTTLE (72189-311-60)
72189-311-72 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, COATED in 1 BOTTLE (72189-311-72)
72189-311-82 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 180 TABLET, COATED in 1 BOTTLE (72189-311-82)
72189-311-84 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 240 TABLET, COATED in 1 BOTTLE (72189-311-84)
72189-311-90 72189-311 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE TRAMADOL HYDROCHLORIDE TABLET, COATED ORAL 20220112 N/A ANDA ANDA208708 DirectRx TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, COATED in 1 BOTTLE (72189-311-90)
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)
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)
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