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
50228-112-30	50228-112	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20140205	N/A	ANDA	ANDA203018	ScieGen Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	50 mg/1	30 TABLET in 1 BOTTLE (50228-112-30)
50228-112-10	50228-112	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20140205	N/A	ANDA	ANDA203018	ScieGen Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	50 mg/1	1000 TABLET in 1 BOTTLE (50228-112-10)
50228-111-30	50228-111	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20140723	N/A	ANDA	ANDA203018	ScieGen Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE (50228-111-30)
50228-111-10	50228-111	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20140723	N/A	ANDA	ANDA203018	ScieGen Pharmaceuticals, Inc.	HYDROCHLOROTHIAZIDE	25 mg/1	1000 TABLET in 1 BOTTLE (50228-111-10)