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
35561-253-10	35561-253	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20200422	N/A	ANDA	ANDA208494	AustarPharma LLC	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (35561-253-10)
35561-253-14	35561-253	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20200422	N/A	ANDA	ANDA208494	AustarPharma LLC	SILDENAFIL CITRATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (35561-253-14)
35561-252-10	35561-252	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20200422	N/A	ANDA	ANDA208494	AustarPharma LLC	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (35561-252-10)
35561-252-14	35561-252	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20200422	N/A	ANDA	ANDA208494	AustarPharma LLC	SILDENAFIL CITRATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (35561-252-14)
82647-212-14	82647-212	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20220328	N/A	ANDA	ANDA208494	Reyoung Corporation	SILDENAFIL CITRATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82647-212-14)
82647-212-30	82647-212	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20220328	N/A	ANDA	ANDA208494	Reyoung Corporation	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82647-212-30)
82647-210-14	82647-210	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20220328	N/A	ANDA	ANDA208494	Reyoung Corporation	SILDENAFIL CITRATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82647-210-14)
82647-210-30	82647-210	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20220328	N/A	ANDA	ANDA208494	Reyoung Corporation	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82647-210-30)
35561-251-10	35561-251	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20200422	N/A	ANDA	ANDA208494	AustarPharma LLC	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (35561-251-10)
35561-251-14	35561-251	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20200422	N/A	ANDA	ANDA208494	AustarPharma LLC	SILDENAFIL CITRATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (35561-251-14)
82647-211-14	82647-211	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20220328	N/A	ANDA	ANDA208494	Reyoung Corporation	SILDENAFIL CITRATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82647-211-14)
82647-211-30	82647-211	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20220328	N/A	ANDA	ANDA208494	Reyoung Corporation	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82647-211-30)