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=ANDA203442"
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
33342-106-07 33342-106 HUMAN PRESCRIPTION DRUG Emtricitabine and tenofovir disoproxil fumarate Emtricitabine and tenofovir disoproxil fumarate TABLET, FILM COATED ORAL 20200515 N/A ANDA ANDA203442 Macleods Pharmaceuticals Limited EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 200 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (33342-106-07)
16714-534-01 16714-534 HUMAN PRESCRIPTION DRUG Emtricitabine and tenofovir disoproxil fumarate Emtricitabine and tenofovir disoproxil fumarate TABLET, FILM COATED ORAL 20220309 N/A ANDA ANDA203442 NorthStar RxLLC EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 200 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-534-01)
68071-3695-3 68071-3695 HUMAN PRESCRIPTION DRUG Emtricitabine and tenofovir disoproxil fumarate Emtricitabine and tenofovir disoproxil fumarate TABLET, FILM COATED ORAL 20241004 N/A ANDA ANDA203442 NuCare Pharmaceuticals, Inc. EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 200 mg/1; 300 mg/1 3 TABLET, FILM COATED in 1 BOTTLE (68071-3695-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase