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
68682-022-90	68682-022	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	25 mg/1	90 TABLET in 1 BOTTLE (68682-022-90)
68682-023-01	68682-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	50 mg/1	1000 TABLET in 1 BOTTLE (68682-023-01)
68682-023-10	68682-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	50 mg/1	100 TABLET in 1 BOTTLE (68682-023-10)
68682-023-50	68682-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	50 mg/1	500 TABLET in 1 BOTTLE (68682-023-50)
68682-023-90	68682-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	50 mg/1	90 TABLET in 1 BOTTLE (68682-023-90)
68682-022-50	68682-022	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	25 mg/1	500 TABLET in 1 BOTTLE (68682-022-50)
68682-022-10	68682-022	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	25 mg/1	100 TABLET in 1 BOTTLE (68682-022-10)
68682-022-01	68682-022	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Oceanside Pharmaceuticals	METHAZOLAMIDE	25 mg/1	1000 TABLET in 1 BOTTLE (68682-022-01)
24208-022-01	24208-022	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Bausch & Lomb Incorporated	METHAZOLAMIDE	25 mg/1	1000 TABLET in 1 BOTTLE (24208-022-01)
24208-023-01	24208-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Bausch & Lomb Incorporated	METHAZOLAMIDE	50 mg/1	1000 TABLET in 1 BOTTLE (24208-023-01)
24208-023-10	24208-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Bausch & Lomb Incorporated	METHAZOLAMIDE	50 mg/1	100 TABLET in 1 BOTTLE (24208-023-10)
24208-023-50	24208-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Bausch & Lomb Incorporated	METHAZOLAMIDE	50 mg/1	500 TABLET in 1 BOTTLE (24208-023-50)
24208-023-90	24208-023	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Bausch & Lomb Incorporated	METHAZOLAMIDE	50 mg/1	90 TABLET in 1 BOTTLE (24208-023-90)
42571-239-05	42571-239	HUMAN PRESCRIPTION DRUG	METHAZOLAMIDE	Methazolamide	TABLET	ORAL	20190305	N/A	ANDA	ANDA207438	Micro Labs Limited	METHAZOLAMIDE	25 mg/1	500 TABLET in 1 BOTTLE (42571-239-05)
42571-239-10	42571-239	HUMAN PRESCRIPTION DRUG	METHAZOLAMIDE	Methazolamide	TABLET	ORAL	20190305	N/A	ANDA	ANDA207438	Micro Labs Limited	METHAZOLAMIDE	25 mg/1	1000 TABLET in 1 BOTTLE (42571-239-10)
42571-239-90	42571-239	HUMAN PRESCRIPTION DRUG	METHAZOLAMIDE	Methazolamide	TABLET	ORAL	20190305	N/A	ANDA	ANDA207438	Micro Labs Limited	METHAZOLAMIDE	25 mg/1	90 TABLET in 1 BOTTLE (42571-239-90)
42571-240-05	42571-240	HUMAN PRESCRIPTION DRUG	METHAZOLAMIDE	Methazolamide	TABLET	ORAL	20190305	N/A	ANDA	ANDA207438	Micro Labs Limited	METHAZOLAMIDE	50 mg/1	500 TABLET in 1 BOTTLE (42571-240-05)
42571-240-10	42571-240	HUMAN PRESCRIPTION DRUG	METHAZOLAMIDE	Methazolamide	TABLET	ORAL	20190305	N/A	ANDA	ANDA207438	Micro Labs Limited	METHAZOLAMIDE	50 mg/1	1000 TABLET in 1 BOTTLE (42571-240-10)
42571-240-90	42571-240	HUMAN PRESCRIPTION DRUG	METHAZOLAMIDE	Methazolamide	TABLET	ORAL	20190305	N/A	ANDA	ANDA207438	Micro Labs Limited	METHAZOLAMIDE	50 mg/1	90 TABLET in 1 BOTTLE (42571-240-90)
24208-022-10	24208-022	HUMAN PRESCRIPTION DRUG	Methazolamide	methazolamide	TABLET	ORAL	20201002	N/A	ANDA	ANDA207438	Bausch & Lomb Incorporated	METHAZOLAMIDE	25 mg/1	100 TABLET in 1 BOTTLE (24208-022-10)