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
0069-4220-30	0069-4220	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	19980327	20290131	NDA	NDA020895	PFIZER LABORATORIES DIV PFIZER INC	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-4220-30)
0069-4220-66	0069-4220	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	19980327	N/A	NDA	NDA020895	PFIZER LABORATORIES DIV PFIZER INC	SILDENAFIL CITRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0069-4220-66)
58151-426-93	58151-426	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	20250715	N/A	NDA	NDA020895	Viatris Specialty LLC	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-426-93)
58151-427-01	58151-427	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	20250805	N/A	NDA	NDA020895	Viatris Specialty LLC	SILDENAFIL CITRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (58151-427-01)
58151-428-93	58151-428	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	20250403	N/A	NDA	NDA020895	Viatris Specialty LLC	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-428-93)
0069-4210-66	0069-4210	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	19980327	20280229	NDA	NDA020895	PFIZER LABORATORIES DIV PFIZER INC	SILDENAFIL CITRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0069-4210-66)
0069-4210-30	0069-4210	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	19980327	N/A	NDA	NDA020895	PFIZER LABORATORIES DIV PFIZER INC	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-4210-30)
0069-4200-30	0069-4200	HUMAN PRESCRIPTION DRUG	Viagra	sildenafil citrate	TABLET, FILM COATED	ORAL	19980327	20270930	NDA	NDA020895	PFIZER LABORATORIES DIV PFIZER INC	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-4200-30)
59762-0034-1	59762-0034	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	sildenafil citrate	TABLET, FILM COATED	ORAL	20171201	N/A	NDA AUTHORIZED GENERIC	NDA020895	Mylan Pharmaceuticals Inc.	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59762-0034-1)
59762-0035-1	59762-0035	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	sildenafil citrate	TABLET, FILM COATED	ORAL	20171201	20261031	NDA AUTHORIZED GENERIC	NDA020895	Mylan Pharmaceuticals Inc.	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59762-0035-1)
59762-0035-2	59762-0035	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	sildenafil citrate	TABLET, FILM COATED	ORAL	20171201	N/A	NDA AUTHORIZED GENERIC	NDA020895	Mylan Pharmaceuticals Inc.	SILDENAFIL CITRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59762-0035-2)
59762-0036-2	59762-0036	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	sildenafil citrate	TABLET, FILM COATED	ORAL	20171201	N/A	NDA AUTHORIZED GENERIC	NDA020895	Mylan Pharmaceuticals Inc.	SILDENAFIL CITRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59762-0036-2)