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
63629-8793-1	63629-8793	HUMAN PRESCRIPTION DRUG	Brinzolamide	Brinzolamide	SUSPENSION/ DROPS	OPHTHALMIC	20210909	N/A	NDA AUTHORIZED GENERIC	NDA020816	Bryant Ranch Prepack	BRINZOLAMIDE	10 mg/mL	1 BOTTLE, PLASTIC in 1 CARTON (63629-8793-1) / 10 mL in 1 BOTTLE, PLASTIC
0078-0722-15	0078-0722	HUMAN PRESCRIPTION DRUG	Azopt	brinzolamide	SUSPENSION/ DROPS	OPHTHALMIC	20211224	N/A	NDA	NDA020816	Novartis Pharmaceuticals Corporation	BRINZOLAMIDE	10 mg/mL	1 BOTTLE in 1 CARTON (0078-0722-15) / 15 mL in 1 BOTTLE
0078-0722-10	0078-0722	HUMAN PRESCRIPTION DRUG	Azopt	brinzolamide	SUSPENSION/ DROPS	OPHTHALMIC	20211224	N/A	NDA	NDA020816	Novartis Pharmaceuticals Corporation	BRINZOLAMIDE	10 mg/mL	1 BOTTLE in 1 CARTON (0078-0722-10) / 10 mL in 1 BOTTLE
0781-6014-70	0781-6014	HUMAN PRESCRIPTION DRUG	Brinzolamide	Brinzolamide	SUSPENSION/ DROPS	OPHTHALMIC	20210308	N/A	NDA AUTHORIZED GENERIC	NDA020816	Sandoz Inc	BRINZOLAMIDE	10 mg/mL	1 BOTTLE, PLASTIC in 1 CARTON (0781-6014-70) / 10 mL in 1 BOTTLE, PLASTIC
0781-6014-85	0781-6014	HUMAN PRESCRIPTION DRUG	Brinzolamide	Brinzolamide	SUSPENSION/ DROPS	OPHTHALMIC	20210308	N/A	NDA AUTHORIZED GENERIC	NDA020816	Sandoz Inc	BRINZOLAMIDE	10 mg/mL	1 BOTTLE, PLASTIC in 1 CARTON (0781-6014-85) / 15 mL in 1 BOTTLE, PLASTIC