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=ANDA208934"
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
71335-1255-4 71335-1255 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240517 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 20 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (71335-1255-4)
71335-1255-5 71335-1255 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240517 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1255-5)
71335-1255-6 71335-1255 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240517 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-1255-6)
71335-1255-7 71335-1255 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240517 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1255-7)
71335-1255-3 71335-1255 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240517 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1255-3)
71335-1255-2 71335-1255 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190621 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-1255-2)
71335-1255-1 71335-1255 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190620 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1255-1)
71335-1884-1 71335-1884 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20210629 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (71335-1884-1)
16714-077-01 16714-077 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200219 N/A ANDA ANDA208934 NorthStar RxLLC TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-077-01)
16714-074-02 16714-074 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200219 N/A ANDA ANDA208934 NorthStar RxLLC TADALAFIL 2.5 mg/1 2 BLISTER PACK in 1 CARTON (16714-074-02) / 15 TABLET, FILM COATED in 1 BLISTER PACK (16714-074-01)
16714-075-01 16714-075 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200219 N/A ANDA ANDA208934 NorthStar RxLLC TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-075-01)
16714-076-01 16714-076 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20200219 N/A ANDA ANDA208934 NorthStar RxLLC TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-076-01)
63629-8157-4 63629-8157 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63629-8157-4)
63629-8157-5 63629-8157 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (63629-8157-5)
63629-8157-6 63629-8157 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA208934 Bryant Ranch Prepack TADALAFIL 10 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (63629-8157-6)
47335-009-64 47335-009 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA208934 Sun Pharmaceutical Industries, Inc. TADALAFIL 2.5 mg/1 2 BLISTER PACK in 1 CARTON (47335-009-64) / 15 TABLET, FILM COATED in 1 BLISTER PACK
47335-010-64 47335-010 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA208934 Sun Pharmaceutical Industries, Inc. TADALAFIL 5 mg/1 2 BLISTER PACK in 1 CARTON (47335-010-64) / 15 TABLET, FILM COATED in 1 BLISTER PACK
47335-010-83 47335-010 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA208934 Sun Pharmaceutical Industries, Inc. TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-010-83)
47335-011-83 47335-011 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA208934 Sun Pharmaceutical Industries, Inc. TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-011-83)
47335-012-83 47335-012 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA208934 Sun Pharmaceutical Industries, Inc. TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-012-83)
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