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
61919-826-10	61919-826	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET, FILM COATED	ORAL	20160829	N/A	ANDA	ANDA203814	DIRECT RX	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (61919-826-10)
61919-826-20	61919-826	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET, FILM COATED	ORAL	20160829	N/A	ANDA	ANDA203814	DIRECT RX	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (61919-826-20)
61919-826-30	61919-826	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET, FILM COATED	ORAL	20220927	N/A	ANDA	ANDA203814	DIRECT RX	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (61919-826-30)
61919-826-50	61919-826	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET, FILM COATED	ORAL	20160829	N/A	ANDA	ANDA203814	DIRECT RX	SILDENAFIL CITRATE	20 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (61919-826-50)
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)
43063-676-10	43063-676	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20160815	20271031	ANDA	ANDA203814	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-676-10)
43063-676-30	43063-676	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20160609	20271031	ANDA	ANDA203814	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-676-30)
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)
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)
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)
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)
33342-536-10	33342-536	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Macleods Pharmaceuticals Limited	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-536-10)