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
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)
51655-820-52	51655-820	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210707	N/A	ANDA	ANDA203814	Northwind Pharmaceuticals	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-820-52)
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)
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)
68071-4517-9	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)
53002-2719-3	53002-2719	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220801	N/A	ANDA	ANDA203814	RPK Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-2719-3)
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)
33342-121-10	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)
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)
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)
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)
76420-061-90	76420-061	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20191210	N/A	ANDA	ANDA203814	Asclemed USA, Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-061-90)
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)
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)
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)