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
51672-4045-1	51672-4045	HUMAN PRESCRIPTION DRUG	Enalapril Maleate and Hydrochlorothiazide	Enalapril Maleate and Hydrochlorothiazide	TABLET	ORAL	20010918	N/A	ANDA	ANDA075788	Taro Pharmaceuticals U.S.A., Inc.	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	5 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (51672-4045-1)
51672-4045-3	51672-4045	HUMAN PRESCRIPTION DRUG	Enalapril Maleate and Hydrochlorothiazide	Enalapril Maleate and Hydrochlorothiazide	TABLET	ORAL	20010918	N/A	ANDA	ANDA075788	Taro Pharmaceuticals U.S.A., Inc.	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	5 mg/1; 12.5 mg/1	1000 TABLET in 1 BOTTLE (51672-4045-3)
51672-4046-1	51672-4046	HUMAN PRESCRIPTION DRUG	Enalapril Maleate and Hydrochlorothiazide	Enalapril Maleate and Hydrochlorothiazide	TABLET	ORAL	20010918	20250101	ANDA	ANDA075788	Taro Pharmaceuticals U.S.A., Inc.	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	10 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (51672-4046-1)
51672-4046-3	51672-4046	HUMAN PRESCRIPTION DRUG	Enalapril Maleate and Hydrochlorothiazide	Enalapril Maleate and Hydrochlorothiazide	TABLET	ORAL	20010918	20250101	ANDA	ANDA075788	Taro Pharmaceuticals U.S.A., Inc.	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	10 mg/1; 25 mg/1	1000 TABLET in 1 BOTTLE (51672-4046-3)
51672-4241-1	51672-4241	HUMAN PRESCRIPTION DRUG	Enalapril Maleate and Hydrochlorothiazide	Enalapril Maleate and Hydrochlorothiazide	TABLET	ORAL	20231120	N/A	ANDA	ANDA075788	Taro Pharmaceuticals U.S.A., Inc.	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	10 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (51672-4241-1)
51672-4241-3	51672-4241	HUMAN PRESCRIPTION DRUG	Enalapril Maleate and Hydrochlorothiazide	Enalapril Maleate and Hydrochlorothiazide	TABLET	ORAL	20231120	N/A	ANDA	ANDA075788	Taro Pharmaceuticals U.S.A., Inc.	ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE	10 mg/1; 25 mg/1	1000 TABLET in 1 BOTTLE (51672-4241-3)