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
63629-9429-1	63629-9429	HUMAN PRESCRIPTION DRUG	Abiraterone Acetate	abiraterone acetate	TABLET, FILM COATED	ORAL	20220823	N/A	ANDA	ANDA215947	Bryant Ranch Prepack	ABIRATERONE ACETATE	250 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-9429-1)
82293-001-10	82293-001	HUMAN PRESCRIPTION DRUG	Abiraterone Acetate	abiraterone acetate	TABLET, FILM COATED	ORAL	20220105	N/A	ANDA	ANDA215947	Novugen Pharma (USA) LLC	ABIRATERONE ACETATE	250 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82293-001-10)
82293-002-10	82293-002	HUMAN PRESCRIPTION DRUG	Abiraterone Acetate	abiraterone acetate	TABLET, FILM COATED	ORAL	20220105	N/A	ANDA	ANDA215947	Novugen Pharma (USA) LLC	ABIRATERONE ACETATE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82293-002-10)
63629-9430-1	63629-9430	HUMAN PRESCRIPTION DRUG	Abiraterone Acetate	abiraterone acetate	TABLET, FILM COATED	ORAL	20220823	N/A	ANDA	ANDA215947	Bryant Ranch Prepack	ABIRATERONE ACETATE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-9430-1)