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
68071-3549-6	68071-3549	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20231204	N/A	ANDA	ANDA206401	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-3549-6)
68071-3549-9	68071-3549	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20240409	N/A	ANDA	ANDA206401	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3549-9)
68071-3592-1	68071-3592	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20250317	N/A	ANDA	ANDA206401	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	25 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-3592-1)
68071-3592-9	68071-3592	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20240405	N/A	ANDA	ANDA206401	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3592-9)
68071-3631-3	68071-3631	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20240617	N/A	ANDA	ANDA206401	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3631-3)
68071-3646-1	68071-3646	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20240716	N/A	ANDA	ANDA206401	NuCare Pharmaceuticals, Inc.	SILDENAFIL CITRATE	50 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-3646-1)
68071-3670-3	68071-3670	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil Citrate	TABLET, FILM COATED	ORAL	20181012	N/A	ANDA	ANDA206401	NuCare Pharmaceuticals, Inc.	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3670-3)
68788-8301-3	68788-8301	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20221130	N/A	ANDA	ANDA206401	Preferred Pharmaceuticals Inc.	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8301-3)
68788-8301-7	68788-8301	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20221130	N/A	ANDA	ANDA206401	Preferred Pharmaceuticals Inc.	SILDENAFIL CITRATE	100 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (68788-8301-7)
68788-8301-1	68788-8301	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20221130	N/A	ANDA	ANDA206401	Preferred Pharmaceuticals Inc.	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68788-8301-1)