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=ANDA201952"
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
42571-119-01 42571-119 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20121215 N/A ANDA ANDA201952 Micro Labs Limited ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (42571-119-01)
42571-119-05 42571-119 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20121215 N/A ANDA ANDA201952 Micro Labs Limited ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (42571-119-05)
42571-119-23 42571-119 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20121215 N/A ANDA ANDA201952 Micro Labs Limited ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 8 BLISTER PACK in 1 CARTON (42571-119-23) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-119-32)
42571-119-90 42571-119 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20121215 N/A ANDA ANDA201952 Micro Labs Limited ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (42571-119-90)
76420-105-01 76420-105 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20201030 N/A ANDA ANDA201952 Asclemed USA, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (76420-105-01)
76420-105-02 76420-105 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20201030 N/A ANDA ANDA201952 Asclemed USA, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 2 TABLET, FILM COATED in 1 BOTTLE (76420-105-02)
76420-105-03 76420-105 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20201030 N/A ANDA ANDA201952 Asclemed USA, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (76420-105-03)
76420-105-10 76420-105 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20201030 N/A ANDA ANDA201952 Asclemed USA, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (76420-105-10)
76420-105-30 76420-105 HUMAN PRESCRIPTION DRUG TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN TABLET, FILM COATED ORAL 20201030 N/A ANDA ANDA201952 Asclemed USA, Inc. ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE 325 mg/1; 37.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-105-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase