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
63629-8991-1	63629-8991	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211207	N/A	ANDA	ANDA040412	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63629-8991-1)
63629-8991-2	63629-8991	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211207	N/A	ANDA	ANDA040412	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (63629-8991-2)
63629-8991-3	63629-8991	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211207	N/A	ANDA	ANDA040412	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (63629-8991-3)
63629-8992-1	63629-8992	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211207	N/A	ANDA	ANDA040412	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	50 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63629-8992-1)
63629-8992-2	63629-8992	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211207	N/A	ANDA	ANDA040412	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	50 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (63629-8992-2)
63629-8992-3	63629-8992	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20211207	N/A	ANDA	ANDA040412	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE	50 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (63629-8992-3)
60687-593-01	60687-593	HUMAN PRESCRIPTION DRUG	Hydrochlorothiazide	Hydrochlorothiazide	TABLET	ORAL	20210312	N/A	ANDA	ANDA040412	American Health Packaging	HYDROCHLOROTHIAZIDE	25 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-593-01) / 1 TABLET in 1 BLISTER PACK (60687-593-11)