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）

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
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)
67296-1657-1	67296-1657	HUMAN PRESCRIPTION DRUG	SULFATRIM	Sulfamethoxazole and Trimethoprim	SUSPENSION	ORAL	19830701	N/A	NDA	NDA018615	RedPharm Drug, Inc.	SULFAMETHOXAZOLE; TRIMETHOPRIM	200 mg/5mL; 40 mg/5mL	100 mL in 1 BOTTLE (67296-1657-1)
67296-1657-2	67296-1657	HUMAN PRESCRIPTION DRUG	SULFATRIM	Sulfamethoxazole and Trimethoprim	SUSPENSION	ORAL	19830701	N/A	NDA	NDA018615	RedPharm Drug, Inc.	SULFAMETHOXAZOLE; TRIMETHOPRIM	200 mg/5mL; 40 mg/5mL	200 mL in 1 BOTTLE (67296-1657-2)
0121-0853-20	0121-0853	HUMAN PRESCRIPTION DRUG	Sulfamethoxazole and Trimethoprim	Sulfamethoxazole and Trimethoprim	SUSPENSION	ORAL	20240805	N/A	NDA	NDA018615	PAI Holdings, LLC dba PAI Pharma	SULFAMETHOXAZOLE; TRIMETHOPRIM	200 mg/5mL; 40 mg/5mL	10 CUP, UNIT-DOSE in 1 TRAY (0121-0853-20) / 20 mL in 1 CUP, UNIT-DOSE
0121-0854-16	0121-0854	HUMAN PRESCRIPTION DRUG	SULFATRIM	Sulfamethoxazole and Trimethoprim	SUSPENSION	ORAL	19830703	N/A	NDA	NDA018615	PAI Holdings, LLC dba PAI Pharma	SULFAMETHOXAZOLE; TRIMETHOPRIM	200 mg/5mL; 40 mg/5mL	473 mL in 1 BOTTLE (0121-0854-16)