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=ANDA209543"
符合检索条件的记录共 4 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
62332-312-30 62332-312 HUMAN PRESCRIPTION DRUG Bosutinib Bosutinib TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA209543 Alembic Pharmaceuticals Inc. BOSUTINIB 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62332-312-30)
62332-311-35 62332-311 HUMAN PRESCRIPTION DRUG Bosutinib Bosutinib TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA209543 Alembic Pharmaceuticals Inc. BOSUTINIB 100 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (62332-311-35)
46708-312-30 46708-312 HUMAN PRESCRIPTION DRUG Bosutinib Bosutinib TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA209543 Alembic Pharmaceuticals Limited BOSUTINIB 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-312-30)
46708-311-35 46708-311 HUMAN PRESCRIPTION DRUG Bosutinib Bosutinib TABLET, FILM COATED ORAL 20260519 N/A ANDA ANDA209543 Alembic Pharmaceuticals Limited BOSUTINIB 100 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (46708-311-35)
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