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=ANDA212231"
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
70069-362-10 70069-362 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20190829 N/A ANDA ANDA212231 Somerset Therapeutics, LLC SULFAMETHOXAZOLE; TRIMETHOPRIM 80 mg/mL; 16 mg/mL 10 VIAL in 1 CARTON (70069-362-10) / 10 mL in 1 VIAL (70069-362-01)
70069-363-01 70069-363 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20190829 N/A ANDA ANDA212231 Somerset Therapeutics, LLC SULFAMETHOXAZOLE; TRIMETHOPRIM 80 mg/mL; 16 mg/mL 1 VIAL in 1 CARTON (70069-363-01) / 30 mL in 1 VIAL
70069-361-10 70069-361 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20190829 N/A ANDA ANDA212231 Somerset Therapeutics, LLC SULFAMETHOXAZOLE; TRIMETHOPRIM 80 mg/mL; 16 mg/mL 10 VIAL in 1 CARTON (70069-361-10) / 5 mL in 1 VIAL (70069-361-01)
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