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
68071-4617-3	68071-4617	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181026	N/A	ANDA	ANDA202659	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4617-3)
68071-4674-3	68071-4674	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181219	N/A	ANDA	ANDA202659	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4674-3)
71335-1028-1	71335-1028	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190712	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1028-1)
71335-1028-2	71335-1028	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181213	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	50 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1028-2)
71335-1028-3	71335-1028	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190711	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1028-3)
71335-1028-4	71335-1028	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1028-4)
71335-1028-5	71335-1028	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20191121	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1028-5)
71335-1028-6	71335-1028	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210907	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1028-6)
71335-1088-0	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1088-0)
71335-1088-1	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1088-1)
71335-1088-2	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (71335-1088-2)
71335-1088-3	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1088-3)
71335-1088-4	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (71335-1088-4)
71335-1088-5	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-1088-5)
71335-1088-6	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1088-6)
71335-1088-7	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (71335-1088-7)
71335-1088-8	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1088-8)
71335-1088-9	71335-1088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA202659	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1088-9)