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=ANDA206401"
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
76420-563-90 76420-563 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-563-90)
76420-564-01 76420-564 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-564-01)
76420-564-30 76420-564 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-564-30)
76420-564-60 76420-564 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-564-60)
76420-564-90 76420-564 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-564-90)
76420-565-01 76420-565 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-565-01)
76420-565-30 76420-565 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-565-30)
76420-565-60 76420-565 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-565-60)
76420-565-90 76420-565 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230510 N/A ANDA ANDA206401 Asclemed USA, Inc. SILDENAFIL CITRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-565-90)
82804-025-30 82804-025 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA206401 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-025-30)
82804-025-60 82804-025 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA206401 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (82804-025-60)
82804-025-90 82804-025 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20231012 N/A ANDA ANDA206401 Proficient Rx LP SILDENAFIL CITRATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82804-025-90)
82009-093-01 82009-093 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230719 N/A ANDA ANDA206401 Quallent Pharmaceuticals Health LLC SILDENAFIL CITRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (82009-093-01)
68788-8301-1 68788-8301 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20221130 N/A ANDA ANDA206401 Preferred Pharmaceuticals Inc. SILDENAFIL CITRATE 100 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68788-8301-1)
68788-8301-3 68788-8301 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20221130 N/A ANDA ANDA206401 Preferred Pharmaceuticals Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8301-3)
68788-8301-7 68788-8301 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20221130 N/A ANDA ANDA206401 Preferred Pharmaceuticals Inc. SILDENAFIL CITRATE 100 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (68788-8301-7)
80425-0410-1 80425-0410 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240710 N/A ANDA ANDA206401 Advanced Rx of Tennessee, LLC SILDENAFIL CITRATE 100 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (80425-0410-1)
80425-0410-2 80425-0410 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240710 N/A ANDA ANDA206401 Advanced Rx of Tennessee, LLC SILDENAFIL CITRATE 100 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (80425-0410-2)
80425-0410-3 80425-0410 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240710 N/A ANDA ANDA206401 Advanced Rx of Tennessee, LLC SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0410-3)
68071-3410-3 68071-3410 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20230518 N/A ANDA ANDA206401 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3410-3)
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