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
51672-4022-1	51672-4022	HUMAN PRESCRIPTION DRUG	Acetazolamide	Acetazolamide	TABLET	ORAL	19970528	N/A	ANDA	ANDA040195	Taro Pharmaceuticals U.S.A., Inc.	ACETAZOLAMIDE	125 mg/1	100 TABLET in 1 BOTTLE (51672-4022-1)
51672-4023-1	51672-4023	HUMAN PRESCRIPTION DRUG	Acetazolamide	Acetazolamide	TABLET	ORAL	19970528	N/A	ANDA	ANDA040195	Taro Pharmaceuticals U.S.A., Inc.	ACETAZOLAMIDE	250 mg/1	100 TABLET in 1 BOTTLE (51672-4023-1)
55289-720-06	55289-720	HUMAN PRESCRIPTION DRUG	Acetazolamide	Acetazolamide	TABLET	ORAL	20160303	N/A	ANDA	ANDA040195	PD-Rx Pharmaceuticals, Inc.	ACETAZOLAMIDE	125 mg/1	6 TABLET in 1 BOTTLE, PLASTIC (55289-720-06)
55289-720-12	55289-720	HUMAN PRESCRIPTION DRUG	Acetazolamide	Acetazolamide	TABLET	ORAL	20160303	N/A	ANDA	ANDA040195	PD-Rx Pharmaceuticals, Inc.	ACETAZOLAMIDE	125 mg/1	12 TABLET in 1 BOTTLE, PLASTIC (55289-720-12)