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=ANDA202659"
符合检索条件的记录共 64 条，共 4 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
70518-1844-1 70518-1844 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20221212 N/A ANDA ANDA202659 REMEDYREPACK INC. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1844-1)
72865-103-01 72865-103 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190801 N/A ANDA ANDA202659 XLCARE Pharmaceuticals INC. SILDENAFIL CITRATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72865-103-01)
72865-103-30 72865-103 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190801 N/A ANDA ANDA202659 XLCARE Pharmaceuticals INC. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72865-103-30)
68071-4674-3 68071-4674 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20181219 N/A ANDA ANDA202659 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4674-3)
50090-5325-0 50090-5325 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20201030 N/A ANDA ANDA202659 A-S Medication Solutions SILDENAFIL CITRATE 100 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-5325-0)
50090-5325-1 50090-5325 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20201030 N/A ANDA ANDA202659 A-S Medication Solutions SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5325-1)
51655-468-54 51655-468 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20201106 N/A ANDA ANDA202659 Northwind Health Company, LLC SILDENAFIL CITRATE 100 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-468-54)
51655-468-87 51655-468 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20201106 N/A ANDA ANDA202659 Northwind Health Company, LLC SILDENAFIL CITRATE 100 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-468-87)
68071-4617-3 68071-4617 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20181026 N/A ANDA ANDA202659 NuCare Pharmaceuticals,Inc. SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4617-3)
31722-710-01 31722-710 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA202659 Camber Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (31722-710-01)
31722-710-05 31722-710 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA202659 Camber Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (31722-710-05)
31722-710-30 31722-710 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20180611 N/A ANDA ANDA202659 Camber Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-710-30)
72865-101-30 72865-101 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190801 N/A ANDA ANDA202659 XLCARE Pharmaceuticals INC. SILDENAFIL CITRATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72865-101-30)
31722-966-01 31722-966 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190801 N/A ANDA ANDA202659 Camber Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (31722-966-01)
31722-966-30 31722-966 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20190801 N/A ANDA ANDA202659 Camber Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-966-30)
72189-069-10 72189-069 HUMAN PRESCRIPTION DRUG SILDENAFIL SILDENAFIL TABLET, FILM COATED ORAL 20200617 N/A ANDA ANDA202659 DIRECT RX SILDENAFIL CITRATE 100 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (72189-069-10)
72189-069-30 72189-069 HUMAN PRESCRIPTION DRUG SILDENAFIL SILDENAFIL TABLET, FILM COATED ORAL 20200617 N/A ANDA ANDA202659 DIRECT RX SILDENAFIL CITRATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-069-30)
50090-5235-0 50090-5235 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20201009 N/A ANDA ANDA202659 A-S Medication Solutions SILDENAFIL CITRATE 25 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-5235-0)
72789-103-15 72789-103 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20200722 N/A ANDA ANDA202659 PD-Rx Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-15)
72789-103-90 72789-103 HUMAN PRESCRIPTION DRUG Sildenafil Sildenafil TABLET, FILM COATED ORAL 20260305 N/A ANDA ANDA202659 PD-Rx Pharmaceuticals, Inc. SILDENAFIL CITRATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-90)
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