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=ANDA213948"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0093-7518-31 0093-7518 HUMAN PRESCRIPTION DRUG fluticasone propionate and salmeterol fluticasone propionate and salmeterol POWDER RESPIRATORY (INHALATION) 20220323 N/A ANDA ANDA213948 Teva Pharmaceuticals USA, Inc. FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 250 ug/1; 50 ug/1 1 POUCH in 1 CARTON (0093-7518-31) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER
0093-7517-31 0093-7517 HUMAN PRESCRIPTION DRUG fluticasone propionate and salmeterol fluticasone propionate and salmeterol POWDER RESPIRATORY (INHALATION) 20220323 N/A ANDA ANDA213948 Teva Pharmaceuticals USA, Inc. FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 100 ug/1; 50 ug/1 1 POUCH in 1 CARTON (0093-7517-31) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER
0093-7516-31 0093-7516 HUMAN PRESCRIPTION DRUG fluticasone propionate and salmeterol fluticasone propionate and salmeterol POWDER RESPIRATORY (INHALATION) 20220323 N/A ANDA ANDA213948 Teva Pharmaceuticals USA, Inc. FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 500 ug/1; 50 ug/1 1 POUCH in 1 CARTON (0093-7516-31) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER
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