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=ANDA208891"
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
0378-9320-32 0378-9320 HUMAN PRESCRIPTION DRUG Wixela Inhub fluticasone propionate and salmeterol POWDER RESPIRATORY (INHALATION) 20190211 N/A ANDA ANDA208891 Mylan Pharmaceuticals Inc. FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 100 ug/1; 50 ug/1 1 INHALER in 1 CARTON (0378-9320-32) / 60 POWDER in 1 INHALER
0378-9321-32 0378-9321 HUMAN PRESCRIPTION DRUG Wixela Inhub fluticasone propionate and salmeterol POWDER RESPIRATORY (INHALATION) 20190211 N/A ANDA ANDA208891 Mylan Pharmaceuticals Inc. FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 250 ug/1; 50 ug/1 1 INHALER in 1 CARTON (0378-9321-32) / 60 POWDER in 1 INHALER
0378-9322-32 0378-9322 HUMAN PRESCRIPTION DRUG Wixela Inhub fluticasone propionate and salmeterol POWDER RESPIRATORY (INHALATION) 20190211 N/A ANDA ANDA208891 Mylan Pharmaceuticals Inc. FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 500 ug/1; 50 ug/1 1 INHALER in 1 CARTON (0378-9322-32) / 60 POWDER in 1 INHALER
70518-2501-0 70518-2501 HUMAN PRESCRIPTION DRUG Wixela Inhub fluticasone propionate and salmeterol POWDER RESPIRATORY (INHALATION) 20191219 N/A ANDA ANDA208891 REMEDYREPACK INC. FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 250 ug/1; 50 ug/1 1 INHALER in 1 CARTON (70518-2501-0) / 60 POWDER in 1 INHALER
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