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
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)
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)
71205-542-30	71205-542	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210311	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-542-30)
71205-542-60	71205-542	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210311	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-542-60)
71205-542-90	71205-542	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210311	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-542-90)
31722-709-05	31722-709	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-709-05)
31722-965-30	31722-965	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-965-30)
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)
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)
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)