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=ANDA214282"
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
70756-721-11 70756-721 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20201113 N/A ANDA ANDA214282 Lifestar Pharma LLC ACETAZOLAMIDE 250 mg/1 100 TABLET in 1 BOTTLE (70756-721-11)
63629-1194-1 63629-1194 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20220208 N/A ANDA ANDA214282 Bryant Ranch Prepack ACETAZOLAMIDE 125 mg/1 100 TABLET in 1 BOTTLE (63629-1194-1)
63629-1195-1 63629-1195 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20220901 N/A ANDA ANDA214282 Bryant Ranch Prepack ACETAZOLAMIDE 250 mg/1 100 TABLET in 1 BOTTLE (63629-1195-1)
72162-1978-1 72162-1978 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20230928 N/A ANDA ANDA214282 Bryant Ranch Prepack ACETAZOLAMIDE 125 mg/1 100 TABLET in 1 BOTTLE (72162-1978-1)
72162-1979-1 72162-1979 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20240125 N/A ANDA ANDA214282 Bryant Ranch Prepack ACETAZOLAMIDE 250 mg/1 100 TABLET in 1 BOTTLE (72162-1979-1)
70756-720-11 70756-720 HUMAN PRESCRIPTION DRUG Acetazolamide Acetazolamide TABLET ORAL 20201113 N/A ANDA ANDA214282 Lifestar Pharma LLC ACETAZOLAMIDE 125 mg/1 100 TABLET in 1 BOTTLE (70756-720-11)
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