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=ANDA209250"
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
71335-2467-1 71335-2467 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-1)
71335-2467-2 71335-2467 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-2)
71335-2467-3 71335-2467 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-3)
71335-2467-4 71335-2467 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-4)
29300-288-01 29300-288 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-288-01)
29300-288-05 29300-288 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-288-05)
29300-288-13 29300-288 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-288-13)
82804-224-30 82804-224 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250521 N/A ANDA ANDA209250 Proficient Rx LP TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-224-30)
82804-224-90 82804-224 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250521 N/A ANDA ANDA209250 Proficient Rx LP TADALAFIL 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-224-90)
76420-854-01 76420-854 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA209250 Asclemed USA, Inc. TADALAFIL 2.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-854-01)
68788-4083-1 68788-4083 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20260227 N/A ANDA ANDA209250 Preferred Pharmaceuticals Inc. TADALAFIL 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4083-1)
68788-4083-3 68788-4083 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20260227 N/A ANDA ANDA209250 Preferred Pharmaceuticals Inc. TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4083-3)
68788-4083-7 68788-4083 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20260227 N/A ANDA ANDA209250 Preferred Pharmaceuticals Inc. TADALAFIL 20 mg/1 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4083-7)
68071-3777-4 68071-3777 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250120 N/A ANDA ANDA209250 NuCare Pharmaceuticals,Inc. TADALAFIL 20 mg/1 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-4)
68071-3777-5 68071-3777 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250120 N/A ANDA ANDA209250 NuCare Pharmaceuticals,Inc. TADALAFIL 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-5)
68071-3777-6 68071-3777 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250421 N/A ANDA ANDA209250 NuCare Pharmaceuticals,Inc. TADALAFIL 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-6)
29300-289-01 29300-289 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-289-01)
29300-289-05 29300-289 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-289-05)
29300-289-13 29300-289 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209250 Unichem Pharmaceuticals (USA), Inc. TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-289-13)
76420-855-01 76420-855 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250128 N/A ANDA ANDA209250 Asclemed USA, Inc. TADALAFIL 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-855-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase