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
0121-0892-63	0121-0892	HUMAN PRESCRIPTION DRUG	Phenytoin	Phenytoin	SUSPENSION	ORAL	20040408	N/A	ANDA	ANDA040521	PAI Holdings, LLC dba PAI Pharma	PHENYTOIN	125 mg/5mL	4 mL in 1 CUP, UNIT-DOSE (0121-0892-63)
17856-4070-1	17856-4070	HUMAN PRESCRIPTION DRUG	Phenytoin	Phenytoin	SUSPENSION	ORAL	20240509	N/A	ANDA	ANDA040521	ATLANTIC BIOLOGICALS CORP.	PHENYTOIN	125 mg/5mL	72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-4070-1) / 4 mL in 1 CUP, UNIT-DOSE (17856-4070-2)
51672-4069-1	51672-4069	HUMAN PRESCRIPTION DRUG	Phenytoin	Phenytoin	SUSPENSION	ORAL	20040408	20260731	ANDA	ANDA040521	Sun Pharmaceutical Industries, Inc.	PHENYTOIN	125 mg/5mL	237 mL in 1 BOTTLE (51672-4069-1)
51672-4069-2	51672-4069	HUMAN PRESCRIPTION DRUG	Phenytoin	Phenytoin	SUSPENSION	ORAL	20250723	N/A	ANDA	ANDA040521	Sun Pharmaceutical Industries, Inc.	PHENYTOIN	125 mg/5mL	1 BOTTLE in 1 CARTON (51672-4069-2) / 237 mL in 1 BOTTLE
60687-275-66	60687-275	HUMAN PRESCRIPTION DRUG	Phenytoin	Phenytoin	SUSPENSION	ORAL	20190110	N/A	ANDA	ANDA040521	American Health Packaging	PHENYTOIN	125 mg/5mL	5 TRAY in 1 CASE (60687-275-66) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-275-63) / 4 mL in 1 CUP, UNIT-DOSE (60687-275-62)