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
71205-231-10	71205-231	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190301	N/A	ANDA	ANDA091448	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-231-10)
71205-231-20	71205-231	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20231019	N/A	ANDA	ANDA091448	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-231-20)
71205-231-30	71205-231	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190301	N/A	ANDA	ANDA091448	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-231-30)
71205-231-60	71205-231	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190301	N/A	ANDA	ANDA091448	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-231-60)
71205-231-90	71205-231	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190301	N/A	ANDA	ANDA091448	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-231-90)