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
47335-038-64	47335-038	HUMAN PRESCRIPTION DRUG	Bosentan	Bosentan	TABLET, FILM COATED	ORAL	20190426	N/A	ANDA	ANDA209324	Sun Pharmaceutical Industries, Inc.	BOSENTAN	62.5 mg/1	10 BLISTER PACK in 1 CARTON (47335-038-64) / 3 TABLET, FILM COATED in 1 BLISTER PACK (47335-038-60)
47335-038-86	47335-038	HUMAN PRESCRIPTION DRUG	Bosentan	Bosentan	TABLET, FILM COATED	ORAL	20190426	N/A	ANDA	ANDA209324	Sun Pharmaceutical Industries, Inc.	BOSENTAN	62.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (47335-038-86)
47335-039-64	47335-039	HUMAN PRESCRIPTION DRUG	Bosentan	Bosentan	TABLET, FILM COATED	ORAL	20190426	N/A	ANDA	ANDA209324	Sun Pharmaceutical Industries, Inc.	BOSENTAN	125 mg/1	10 BLISTER PACK in 1 CARTON (47335-039-64) / 3 TABLET, FILM COATED in 1 BLISTER PACK (47335-039-60)
47335-039-86	47335-039	HUMAN PRESCRIPTION DRUG	Bosentan	Bosentan	TABLET, FILM COATED	ORAL	20190426	N/A	ANDA	ANDA209324	Sun Pharmaceutical Industries, Inc.	BOSENTAN	125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (47335-039-86)