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=NDA018615"
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
0121-0853-40 0121-0853 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim SUSPENSION ORAL 20180829 N/A NDA NDA018615 Pharmaceutical Associates, Inc. SULFAMETHOXAZOLE; TRIMETHOPRIM 200 mg/5mL; 40 mg/5mL 4 TRAY in 1 CASE (0121-0853-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 20 mL in 1 CUP, UNIT-DOSE (0121-0853-20)
0121-0853-00 0121-0853 HUMAN PRESCRIPTION DRUG Sulfamethoxazole and Trimethoprim Sulfamethoxazole and Trimethoprim SUSPENSION ORAL 20180829 N/A NDA NDA018615 Pharmaceutical Associates, Inc. SULFAMETHOXAZOLE; TRIMETHOPRIM 200 mg/5mL; 40 mg/5mL 10 TRAY in 1 CASE (0121-0853-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 20 mL in 1 CUP, UNIT-DOSE (0121-0853-20)
0121-0854-16 0121-0854 HUMAN PRESCRIPTION DRUG SULFATRIM Sulfamethoxazole and Trimethoprim SUSPENSION ORAL 19830701 N/A NDA NDA018615 PAI Holdings, LLC SULFAMETHOXAZOLE; TRIMETHOPRIM 200 mg/5mL; 40 mg/5mL 473 mL in 1 BOTTLE (0121-0854-16)
68788-7345-4 68788-7345 HUMAN PRESCRIPTION DRUG SULFATRIM Sulfamethoxazole and Trimethoprim SUSPENSION ORAL 20200601 N/A NDA NDA018615 Preferred Pharmaceuticals, Inc. SULFAMETHOXAZOLE; TRIMETHOPRIM 200 mg/5mL; 40 mg/5mL 473 mL in 1 BOTTLE (68788-7345-4)
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