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=ANDA217606"
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
82968-005-01 82968-005 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240821 N/A ANDA ANDA217606 FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82968-005-01)
82968-002-01 82968-002 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240821 N/A ANDA ANDA217606 FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82968-002-01)
82968-002-02 82968-002 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240821 N/A ANDA ANDA217606 FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED TADALAFIL 5 mg/1 2 BLISTER PACK in 1 CARTON (82968-002-02) / 15 TABLET, FILM COATED in 1 BLISTER PACK
82968-003-01 82968-003 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240821 N/A ANDA ANDA217606 FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82968-003-01)
82968-001-03 82968-001 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240821 N/A ANDA ANDA217606 FOURRTS (INDIA) LABORATORIES PRIVATE LIMITED TADALAFIL 2.5 mg/1 2 BLISTER PACK in 1 CARTON (82968-001-03) / 15 TABLET, FILM COATED in 1 BLISTER PACK
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