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
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)
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)
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)
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)
68071-3646-1 68071-3646 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil TABLET, FILM COATED ORAL 20240716 N/A ANDA ANDA206401 NuCare Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (68071-3646-1)
76420-563-30 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 30 TABLET, FILM COATED in 1 BOTTLE (76420-563-30)
76420-563-60 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 60 TABLET, FILM COATED in 1 BOTTLE (76420-563-60)
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)
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