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=ANDA209539"
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
69097-373-94 69097-373 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 2.5 mg/1 2 BLISTER PACK in 1 CARTON (69097-373-94) / 15 TABLET, FILM COATED in 1 BLISTER PACK (69097-373-56)
69097-374-02 69097-374 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69097-374-02)
69097-374-05 69097-374 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (69097-374-05)
69097-374-15 69097-374 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69097-374-15)
69097-373-15 69097-373 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 2.5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69097-373-15)
69097-373-05 69097-373 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 2.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (69097-373-05)
69097-373-02 69097-373 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 2.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69097-373-02)
69097-374-94 69097-374 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 5 mg/1 2 BLISTER PACK in 1 CARTON (69097-374-94) / 15 TABLET, FILM COATED in 1 BLISTER PACK (69097-374-56)
69097-376-02 69097-376 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69097-376-02)
69097-376-05 69097-376 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (69097-376-05)
69097-376-15 69097-376 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69097-376-15)
69097-375-02 69097-375 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69097-375-02)
69097-375-05 69097-375 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (69097-375-05)
69097-375-15 69097-375 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209539 Cipla USA Inc. TADALAFIL 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69097-375-15)
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