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
62756-368-08	62756-368	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-368-08)
62756-368-18	62756-368	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 100 mg/1	1000 TABLET in 1 BOTTLE (62756-368-18)
62756-368-83	62756-368	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 100 mg/1	30 TABLET in 1 BOTTLE (62756-368-83)
62756-368-88	62756-368	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-368-88)
62756-369-08	62756-369	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	50 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-369-08)
62756-369-18	62756-369	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	50 mg/1; 100 mg/1	1000 TABLET in 1 BOTTLE (62756-369-18)
62756-369-83	62756-369	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	50 mg/1; 100 mg/1	30 TABLET in 1 BOTTLE (62756-369-83)
62756-369-88	62756-369	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	50 mg/1; 100 mg/1	100 TABLET in 1 BOTTLE (62756-369-88)
62756-370-08	62756-370	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 50 mg/1	100 TABLET in 1 BOTTLE (62756-370-08)
62756-370-18	62756-370	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 50 mg/1	1000 TABLET in 1 BOTTLE (62756-370-18)
62756-370-83	62756-370	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 50 mg/1	30 TABLET in 1 BOTTLE (62756-370-83)
62756-370-88	62756-370	HUMAN PRESCRIPTION DRUG	Metoprolol Tartrate and Hydrochlorothiazide	Metoprolol Tartrate and Hydrochlorothiazide	TABLET	ORAL	20220401	N/A	ANDA	ANDA090654	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE	25 mg/1; 50 mg/1	100 TABLET in 1 BOTTLE (62756-370-88)