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
82804-082-90	82804-082	HUMAN PRESCRIPTION DRUG	bicalutamide	bicalutamide	TABLET, FILM COATED	ORAL	20240313	N/A	ANDA	ANDA079110	Proficient Rx LP	BICALUTAMIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-082-90)
47335-485-18	47335-485	HUMAN PRESCRIPTION DRUG	bicalutamide	bicalutamide	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA079110	Sun Pharmaceutical Industries, Inc.	BICALUTAMIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-485-18)
47335-485-83	47335-485	HUMAN PRESCRIPTION DRUG	bicalutamide	bicalutamide	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA079110	Sun Pharmaceutical Industries, Inc.	BICALUTAMIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-485-83)
47335-485-88	47335-485	HUMAN PRESCRIPTION DRUG	bicalutamide	bicalutamide	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA079110	Sun Pharmaceutical Industries, Inc.	BICALUTAMIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-485-88)
47335-485-08	47335-485	HUMAN PRESCRIPTION DRUG	bicalutamide	bicalutamide	TABLET, FILM COATED	ORAL	20141215	N/A	ANDA	ANDA079110	Sun Pharmaceutical Industries, Inc.	BICALUTAMIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-485-08)