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=ANDA089175"
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
62135-751-01 62135-751 HUMAN PRESCRIPTION DRUG BUTALBITAL, ACETAMINOPHEN AND CAFFEINE BUTALBITAL, ACETAMINOPHEN AND CAFFEINE TABLET ORAL 20230825 N/A ANDA ANDA089175 Chartwell RX, LLC ACETAMINOPHEN; BUTALBITAL; CAFFEINE 325 mg/1; 50 mg/1; 40 mg/1 100 TABLET in 1 BOTTLE (62135-751-01)
63187-520-30 63187-520 HUMAN PRESCRIPTION DRUG butalbital, acetaminophen and caffeine butalbital, acetaminophen and caffeine TABLET ORAL 20181201 N/A ANDA ANDA089175 Proficient Rx LP ACETAMINOPHEN; BUTALBITAL; CAFFEINE 325 mg/1; 50 mg/1; 40 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (63187-520-30)
63187-520-60 63187-520 HUMAN PRESCRIPTION DRUG butalbital, acetaminophen and caffeine butalbital, acetaminophen and caffeine TABLET ORAL 20181201 N/A ANDA ANDA089175 Proficient Rx LP ACETAMINOPHEN; BUTALBITAL; CAFFEINE 325 mg/1; 50 mg/1; 40 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (63187-520-60)
63187-520-90 63187-520 HUMAN PRESCRIPTION DRUG butalbital, acetaminophen and caffeine butalbital, acetaminophen and caffeine TABLET ORAL 20181201 N/A ANDA ANDA089175 Proficient Rx LP ACETAMINOPHEN; BUTALBITAL; CAFFEINE 325 mg/1; 50 mg/1; 40 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (63187-520-90)
46672-053-10 46672-053 HUMAN PRESCRIPTION DRUG butalbital, acetaminophen and caffeine butalbital, acetaminophen and caffeine TABLET ORAL 19870121 N/A ANDA ANDA089175 Mikart, LLC ACETAMINOPHEN; BUTALBITAL; CAFFEINE 325 mg/1; 50 mg/1; 40 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (46672-053-10)
46672-053-50 46672-053 HUMAN PRESCRIPTION DRUG butalbital, acetaminophen and caffeine butalbital, acetaminophen and caffeine TABLET ORAL 19870121 N/A ANDA ANDA089175 Mikart, LLC ACETAMINOPHEN; BUTALBITAL; CAFFEINE 325 mg/1; 50 mg/1; 40 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (46672-053-50)
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