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
72786-101-01	72786-101	HUMAN PRESCRIPTION DRUG	OXBRYTA	Voxelotor	TABLET, FILM COATED	ORAL	20191125	N/A	NDA	NDA213137	Global Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.	VOXELOTOR	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72786-101-01)
72786-102-02	72786-102	HUMAN PRESCRIPTION DRUG	OXBRYTA	Voxelotor	TABLET, FILM COATED	ORAL	20221014	N/A	NDA	NDA213137	Global Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.	VOXELOTOR	300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72786-102-02)
72786-102-03	72786-102	HUMAN PRESCRIPTION DRUG	OXBRYTA	Voxelotor	TABLET, FILM COATED	ORAL	20221014	N/A	NDA	NDA213137	Global Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.	VOXELOTOR	300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72786-102-03)