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
71335-1638-4	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1638-4)
71335-1638-5	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1638-5)
71335-1638-6	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1638-6)
71335-1638-7	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71335-1638-7)
71335-1638-8	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1638-8)
71335-1638-9	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (71335-1638-9)
68001-363-05	68001-363	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180914	20271031	ANDA	ANDA203814	BluePoint Laboratories	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68001-363-05)
63187-813-60	63187-813	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA203814	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-813-60)
63187-813-90	63187-813	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA203814	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-813-90)
63187-813-10	63187-813	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA203814	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63187-813-10)
63187-813-30	63187-813	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA203814	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-813-30)
63187-813-50	63187-813	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170201	N/A	ANDA	ANDA203814	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (63187-813-50)
68001-597-05	68001-597	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20230612	N/A	ANDA	ANDA203814	BluePoint Laboratories	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68001-597-05)
68071-2072-5	68071-2072	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170124	20271031	ANDA	ANDA203814	NuCare Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-2072-5)
68071-2072-1	68071-2072	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170124	20271031	ANDA	ANDA203814	NuCare Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-2072-1)
68071-2072-2	68071-2072	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170124	20271031	ANDA	ANDA203814	NuCare Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68071-2072-2)
68071-2072-4	68071-2072	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20170124	20271031	ANDA	ANDA203814	NuCare Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (68071-2072-4)
60687-788-21	60687-788	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20231113	N/A	ANDA	ANDA203814	American Health Packaging	SILDENAFIL CITRATE	20 mg/1	30 BLISTER PACK in 1 CARTON (60687-788-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-788-11)
33342-121-10	33342-121	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	20271031	ANDA	ANDA203814	Macleods Pharmaceuticals Limited	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-121-10)
33342-121-12	33342-121	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	20271031	ANDA	ANDA203814	Macleods Pharmaceuticals Limited	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BLISTER PACK (33342-121-12)