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）
检索条件:" 注册申请号=NDA209935"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0078-0909-61 0078-0909 HUMAN PRESCRIPTION DRUG KISQALI FEMARA CO-PACK letrozole and ribociclib KIT 20170504 N/A NDA NDA209935 Novartis Pharmaceuticals Corporation 1 KIT in 1 KIT (0078-0909-61) * 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0881-50) * 21 TABLET in 1 BLISTER PACK (0078-0888-21)
0078-0923-61 0078-0923 HUMAN PRESCRIPTION DRUG KISQALI FEMARA CO-PACK letrozole and ribociclib KIT 20170504 N/A NDA NDA209935 Novartis Pharmaceuticals Corporation 1 KIT in 1 KIT (0078-0923-61) * 21 TABLET in 1 BLISTER PACK (0078-0902-21) * 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0881-50)
0078-0916-61 0078-0916 HUMAN PRESCRIPTION DRUG KISQALI FEMARA CO-PACK letrozole and ribociclib KIT 20170504 N/A NDA NDA209935 Novartis Pharmaceuticals Corporation 1 KIT in 1 KIT (0078-0916-61) * 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0078-0881-50) * 14 TABLET in 1 BLISTER PACK (0078-0895-14)
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