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
0078-0860-01	0078-0860	HUMAN PRESCRIPTION DRUG	KISQALI	ribociclib	TABLET, FILM COATED	ORAL	20170313	N/A	NDA	NDA209092	Novartis Pharmaceuticals Corporation	RIBOCICLIB SUCCINATE	200 mg/1	1 BLISTER PACK in 1 CARTON (0078-0860-01) / 21 TABLET, FILM COATED in 1 BLISTER PACK
0078-0867-42	0078-0867	HUMAN PRESCRIPTION DRUG	KISQALI	ribociclib	TABLET, FILM COATED	ORAL	20170313	N/A	NDA	NDA209092	Novartis Pharmaceuticals Corporation	RIBOCICLIB SUCCINATE	200 mg/1	3 BLISTER PACK in 1 CARTON (0078-0867-42) / 14 TABLET, FILM COATED in 1 BLISTER PACK (0078-0867-14)
0078-0874-63	0078-0874	HUMAN PRESCRIPTION DRUG	KISQALI	ribociclib	TABLET, FILM COATED	ORAL	20170313	N/A	NDA	NDA209092	Novartis Pharmaceuticals Corporation	RIBOCICLIB SUCCINATE	200 mg/1	3 BLISTER PACK in 1 CARTON (0078-0874-63) / 21 TABLET, FILM COATED in 1 BLISTER PACK (0078-0874-21)