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=ANDA216383"
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
70954-408-10 70954-408 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil Citrate TABLET ORAL 20230829 N/A ANDA ANDA216383 ANI Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET in 1 BOTTLE (70954-408-10)
70954-407-10 70954-407 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil Citrate TABLET ORAL 20230829 N/A ANDA ANDA216383 ANI Pharmaceuticals, Inc. SILDENAFIL CITRATE 25 mg/1 30 TABLET in 1 BOTTLE (70954-407-10)
70954-409-10 70954-409 HUMAN PRESCRIPTION DRUG Sildenafil Citrate Sildenafil Citrate TABLET ORAL 20230829 N/A ANDA ANDA216383 ANI Pharmaceuticals, Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET in 1 BOTTLE (70954-409-10)
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