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）

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
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)
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)
71335-1088-0	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1088-0)
71335-1088-1	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1088-1)
71335-1088-2	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (71335-1088-2)
71335-1088-3	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1088-3)
71335-1088-4	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (71335-1088-4)
71335-1088-5	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-1088-5)
72789-098-10	72789-098	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200715	N/A	ANDA	ANDA202659	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-10)
72789-098-15	72789-098	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200804	N/A	ANDA	ANDA202659	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-15)
72789-098-90	72789-098	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20240521	N/A	ANDA	ANDA202659	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-098-90)
31722-711-01	31722-711	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-711-01)
31722-711-05	31722-711	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-711-05)
31722-711-30	31722-711	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-711-30)
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)
68071-4599-1	68071-4599	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181012	N/A	ANDA	ANDA202659	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-4599-1)
68071-4599-5	68071-4599	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181012	N/A	ANDA	ANDA202659	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68071-4599-5)