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
68071-2566-3	68071-2566	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20211105	N/A	ANDA	ANDA203623	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2566-3)
63187-619-10	63187-619	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA203623	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63187-619-10)
63187-619-30	63187-619	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA203623	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-619-30)
63187-619-60	63187-619	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA203623	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-619-60)
63187-619-90	63187-619	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA203623	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-619-90)
71335-1649-0	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220301	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-1649-0)
71335-1649-1	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200709	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1649-1)
71335-1649-2	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200624	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1649-2)
71335-1649-3	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210510	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-1649-3)
71335-1649-4	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200623	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1649-4)
71335-1649-5	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210331	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1649-5)
71335-1649-6	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200813	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1649-6)
71335-1649-7	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20240530	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71335-1649-7)
71335-1649-8	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20210712	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1649-8)
71335-1649-9	71335-1649	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20240530	N/A	ANDA	ANDA203623	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (71335-1649-9)
50090-5236-0	50090-5236	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201009	N/A	ANDA	ANDA203623	A-S Medication Solutions	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5236-0)
50090-5236-1	50090-5236	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201009	N/A	ANDA	ANDA203623	A-S Medication Solutions	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5236-1)
63739-072-33	63739-072	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220329	N/A	ANDA	ANDA203623	McKesson Corporation dba SKY Packaging	SILDENAFIL CITRATE	20 mg/1	3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-072-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68071-2213-9	68071-2213	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20200708	N/A	ANDA	ANDA203623	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2213-9)
53002-3719-3	53002-3719	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA203623	RPK Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-3719-3)