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=ANDA219400"
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
39822-9300-2 39822-9300 HUMAN PRESCRIPTION DRUG Dehydrated Alcohol Alcohol INJECTION, SOLUTION PERCUTANEOUS 20250624 N/A ANDA ANDA219400 XGen Pharmaceuticals DJB, Inc. ALCOHOL 1 mL/mL 10 AMPULE in 1 CARTON (39822-9300-2) / 5 mL in 1 AMPULE (39822-9300-1)
50090-7643-0 50090-7643 HUMAN PRESCRIPTION DRUG Dehydrated Alcohol Alcohol INJECTION, SOLUTION PERCUTANEOUS 20250827 N/A ANDA ANDA219400 A-S Medication Solutions ALCOHOL 1 mL/mL 1 AMPULE in 1 CARTON (50090-7643-0) / 5 mL in 1 AMPULE
50090-7643-1 50090-7643 HUMAN PRESCRIPTION DRUG Dehydrated Alcohol Alcohol INJECTION, SOLUTION PERCUTANEOUS 20250827 N/A ANDA ANDA219400 A-S Medication Solutions ALCOHOL 1 mL/mL 2 AMPULE in 1 CARTON (50090-7643-1) / 5 mL in 1 AMPULE
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