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)
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)