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=ANDA217880"
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
70710-1930-6 70710-1930 HUMAN PRESCRIPTION DRUG Maraviroc Maraviroc TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA217880 Zydus Pharmaceuticals USA Inc. MARAVIROC 150 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (70710-1930-6)
68475-008-01 68475-008 HUMAN PRESCRIPTION DRUG Maraviroc Maraviroc TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA217880 Navinta LLC MARAVIROC 150 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68475-008-01)
70710-1931-6 70710-1931 HUMAN PRESCRIPTION DRUG Maraviroc Maraviroc TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA217880 Zydus Pharmaceuticals USA Inc. MARAVIROC 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (70710-1931-6)
68475-007-01 68475-007 HUMAN PRESCRIPTION DRUG Maraviroc Maraviroc TABLET, FILM COATED ORAL 20250623 N/A ANDA ANDA217880 Navinta LLC MARAVIROC 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68475-007-01)
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