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"
符合检索条件的记录共 50 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
76420-565-90 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)
50090-5906-0 50090-5906 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20220117 N/A ANDA ANDA206401 A-S Medication Solutions SILDENAFIL CITRATE 25 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-5906-0)
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)
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)
27241-069-03 27241-069 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20181012 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (27241-069-03)
27241-069-05 27241-069 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240729 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (27241-069-05)
27241-069-10 27241-069 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20181012 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (27241-069-10)
27241-068-03 27241-068 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20181012 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (27241-068-03)
27241-068-05 27241-068 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240729 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (27241-068-05)
27241-068-10 27241-068 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20181012 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (27241-068-10)
27241-067-03 27241-067 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20181012 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (27241-067-03)
27241-067-05 27241-067 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240729 N/A ANDA ANDA206401 Ajanta Pharma USA Inc. SILDENAFIL CITRATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (27241-067-05)
68071-3592-1 68071-3592 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20250317 N/A ANDA ANDA206401 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 25 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68071-3592-1)
68071-3592-9 68071-3592 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240405 N/A ANDA ANDA206401 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3592-9)
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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