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
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)
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)
60687-416-21	60687-416	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190219	20250630	ANDA	ANDA203814	American Health Packaging	SILDENAFIL CITRATE	20 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-416-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-416-11)
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)
71335-1638-1	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1638-1)
71335-1638-2	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1638-2)
71335-1638-3	71335-1638	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-1638-3)
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)
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)
33342-536-58	33342-536	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA203814	Macleods Pharmaceuticals Limited	SILDENAFIL CITRATE	20 mg/1	6500 TABLET, FILM COATED in 1 POUCH (33342-536-58)
33342-536-66	33342-536	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20140103	N/A	ANDA	ANDA203814	Macleods Pharmaceuticals Limited	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BLISTER PACK (33342-536-66)
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)
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)
76420-061-30	76420-061	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20191210	N/A	ANDA	ANDA203814	Asclemed USA, Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-061-30)
76420-061-60	76420-061	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220831	N/A	ANDA	ANDA203814	Asclemed USA, Inc.	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-061-60)