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=ANDA216999"
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
46122-742-68 46122-742 HUMAN OTC DRUG Acetaminophen and Ibuprofen Acetaminophen and Ibuprofen TABLET, FILM COATED ORAL 20230908 N/A ANDA ANDA216999 AMERISOURCE BERGEN ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 36 TABLET, FILM COATED in 1 CARTON (46122-742-68)
69452-394-64 69452-394 HUMAN OTC DRUG Acetaminophen and Ibuprofen Acetaminophen and Ibuprofen TABLET, FILM COATED ORAL 20230908 N/A ANDA ANDA216999 Bionpharma Inc. ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 216 TABLET, FILM COATED in 1 BOTTLE (69452-394-64)
53943-034-76 53943-034 HUMAN OTC DRUG Acetaminophen and Ibuprofen Acetaminophen and Ibuprofen TABLET, FILM COATED ORAL 20230908 N/A ANDA ANDA216999 DISCOUNT DRUG MART, INC. ACETAMINOPHEN; IBUPROFEN 250 mg/1; 125 mg/1 72 TABLET, FILM COATED in 1 CARTON (53943-034-76)
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