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 3 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
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)
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)
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)
72189-311-60 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)
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)
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)
70518-3824-0 70518-3824 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230807 N/A ANDA ANDA208708 REMEDYREPACK INC. TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BLISTER PACK (70518-3824-0)
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)
67046-1541-3 67046-1541 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250325 N/A ANDA ANDA208708 Coupler LLC TRAMADOL HYDROCHLORIDE 100 mg/1 30 TABLET, COATED in 1 BLISTER PACK (67046-1541-3)
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)
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