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
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)
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)
68071-5115-6	68071-5115	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	20271031	ANDA	ANDA203814	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-5115-6)
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)
45865-833-30	45865-833	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA203814	Medsource Pharmaceuticals	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (45865-833-30)
68071-4517-9	68071-4517	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180803	20271031	ANDA	ANDA203814	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-4517-9)
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)
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)
71335-1005-3	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-1005-3)
71335-1005-4	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1005-4)
71335-1005-5	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1005-5)
71335-1005-6	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1005-6)
71335-1005-7	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71335-1005-7)
71335-1005-8	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1005-8)
71335-1005-9	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (71335-1005-9)
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)
71335-1005-1	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1005-1)
71335-1005-2	71335-1005	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20161014	20271031	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1005-2)