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
0002-4732-30	0002-4732	HUMAN PRESCRIPTION DRUG	Olumiant	baricitinib	TABLET, FILM COATED	ORAL	20191008	N/A	NDA	NDA207924	Eli Lilly and Company	BARICITINIB	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0002-4732-30)
0002-4479-30	0002-4479	HUMAN PRESCRIPTION DRUG	Olumiant	baricitinib	TABLET, FILM COATED	ORAL	20220510	N/A	NDA	NDA207924	Eli Lilly and Company	BARICITINIB	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0002-4479-30)
0002-4479-61	0002-4479	HUMAN PRESCRIPTION DRUG	Olumiant	baricitinib	TABLET, FILM COATED	ORAL	20220510	N/A	NDA	NDA207924	Eli Lilly and Company	BARICITINIB	4 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0002-4479-61)
0002-4182-30	0002-4182	HUMAN PRESCRIPTION DRUG	Olumiant	baricitinib	TABLET, FILM COATED	ORAL	20180531	N/A	NDA	NDA207924	Eli Lilly and Company	BARICITINIB	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0002-4182-30)
0002-4182-61	0002-4182	HUMAN PRESCRIPTION DRUG	Olumiant	baricitinib	TABLET, FILM COATED	ORAL	20180531	N/A	NDA	NDA207924	Eli Lilly and Company	BARICITINIB	2 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0002-4182-61)