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
72789-103-15	72789-103	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200722	N/A	ANDA	ANDA202659	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-103-15)
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)
71335-1088-9	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)
31722-711-01	31722-711	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-711-01)
31722-711-05	31722-711	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-711-05)
31722-711-30	31722-711	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA202659	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-711-30)
70518-1844-1	70518-1844	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20221212	N/A	ANDA	ANDA202659	REMEDYREPACK INC.	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1844-1)
71205-498-02	71205-498	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20211028	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (71205-498-02)
71205-498-10	71205-498	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201028	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-498-10)
71205-498-20	71205-498	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201028	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-498-20)
71205-498-30	71205-498	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201028	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-498-30)
71205-498-60	71205-498	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201028	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-498-60)
71205-498-90	71205-498	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201028	N/A	ANDA	ANDA202659	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-498-90)