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=NDA210868"
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
0069-0231-01 0069-0231 HUMAN PRESCRIPTION DRUG Lorbrena lorlatinib TABLET, FILM COATED ORAL 20181119 N/A NDA NDA210868 Pfizer Laboratories Div Pfizer Inc LORLATINIB 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0069-0231-01)
0069-0227-03 0069-0227 HUMAN PRESCRIPTION DRUG Lorbrena lorlatinib TABLET, FILM COATED ORAL 20250103 N/A NDA NDA210868 Pfizer Laboratories Div Pfizer Inc LORLATINIB 25 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (0069-0227-03)
0069-0227-01 0069-0227 HUMAN PRESCRIPTION DRUG Lorbrena lorlatinib TABLET, FILM COATED ORAL 20181119 N/A NDA NDA210868 Pfizer Laboratories Div Pfizer Inc LORLATINIB 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0069-0227-01)
63539-927-01 63539-927 HUMAN PRESCRIPTION DRUG Lorbrena lorlatinib TABLET, FILM COATED ORAL 20230103 N/A NDA NDA210868 U.S. Pharmaceuticals LORLATINIB 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63539-927-01)
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