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
70710-1238-1	70710-1238	HUMAN PRESCRIPTION DRUG	acetaZOLAMIDE	acetaZOLAMIDE	TABLET	ORAL	20230804	N/A	ANDA	ANDA211069	Zydus Pharmaceuticals (USA) Inc.	ACETAZOLAMIDE	125 mg/1	100 TABLET in 1 BOTTLE (70710-1238-1)
70710-1239-1	70710-1239	HUMAN PRESCRIPTION DRUG	acetaZOLAMIDE	acetaZOLAMIDE	TABLET	ORAL	20230804	N/A	ANDA	ANDA211069	Zydus Pharmaceuticals (USA) Inc.	ACETAZOLAMIDE	250 mg/1	100 TABLET in 1 BOTTLE (70710-1239-1)
72578-149-01	72578-149	HUMAN PRESCRIPTION DRUG	acetaZOLAMIDE	acetaZOLAMIDE	TABLET	ORAL	20230715	N/A	ANDA	ANDA211069	Viona Pharmaceuticals Inc	ACETAZOLAMIDE	125 mg/1	100 TABLET in 1 BOTTLE (72578-149-01)
72578-150-01	72578-150	HUMAN PRESCRIPTION DRUG	acetaZOLAMIDE	acetaZOLAMIDE	TABLET	ORAL	20230715	N/A	ANDA	ANDA211069	Viona Pharmaceuticals Inc	ACETAZOLAMIDE	250 mg/1	100 TABLET in 1 BOTTLE (72578-150-01)
70771-1827-1	70771-1827	HUMAN PRESCRIPTION DRUG	acetaZOLAMIDE	acetaZOLAMIDE	TABLET	ORAL	20230715	N/A	ANDA	ANDA211069	Zydus Lifesciences Limited	ACETAZOLAMIDE	125 mg/1	100 TABLET in 1 BOTTLE (70771-1827-1)
70771-1828-1	70771-1828	HUMAN PRESCRIPTION DRUG	acetaZOLAMIDE	acetaZOLAMIDE	TABLET	ORAL	20230715	N/A	ANDA	ANDA211069	Zydus Lifesciences Limited	ACETAZOLAMIDE	250 mg/1	100 TABLET in 1 BOTTLE (70771-1828-1)