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
59762-5000-5	59762-5000	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20200413	N/A	NDA AUTHORIZED GENERIC	NDA007073	Greenstone LLC	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (59762-5000-5) / 100 TABLET in 1 BOTTLE
59762-5000-6	59762-5000	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20200413	N/A	NDA AUTHORIZED GENERIC	NDA007073	Greenstone LLC	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (59762-5000-6) / 300 TABLET in 1 BOTTLE
70518-1829-3	70518-1829	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20211029	N/A	NDA AUTHORIZED GENERIC	NDA007073	REMEDYREPACK INC.	SULFASALAZINE	500 mg/1	30 TABLET in 1 BLISTER PACK (70518-1829-3)
0013-0101-10	0013-0101	HUMAN PRESCRIPTION DRUG	Azulfidine	Sulfasalazine	TABLET	ORAL	20200227	N/A	NDA	NDA007073	Pfizer Laboratories Div Pfizer Inc	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (0013-0101-10) / 100 TABLET in 1 BOTTLE
0013-0101-30	0013-0101	HUMAN PRESCRIPTION DRUG	Azulfidine	Sulfasalazine	TABLET	ORAL	20200227	N/A	NDA	NDA007073	Pfizer Laboratories Div Pfizer Inc	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (0013-0101-30) / 300 TABLET in 1 BOTTLE
50090-6936-0	50090-6936	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20231215	N/A	NDA AUTHORIZED GENERIC	NDA007073	A-S Medication Solutions	SULFASALAZINE	500 mg/1	90 TABLET in 1 BOTTLE (50090-6936-0)
50090-0086-0	50090-0086	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20181128	N/A	NDA AUTHORIZED GENERIC	NDA007073	A-S Medication Solutions	SULFASALAZINE	500 mg/1	50 TABLET in 1 BOTTLE (50090-0086-0)
50090-0086-3	50090-0086	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20141128	N/A	NDA AUTHORIZED GENERIC	NDA007073	A-S Medication Solutions	SULFASALAZINE	500 mg/1	30 TABLET in 1 BOTTLE (50090-0086-3)
50090-0086-4	50090-0086	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20211110	N/A	NDA AUTHORIZED GENERIC	NDA007073	A-S Medication Solutions	SULFASALAZINE	500 mg/1	90 TABLET in 1 BOTTLE (50090-0086-4)
71610-706-70	71610-706	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20230516	N/A	NDA AUTHORIZED GENERIC	NDA007073	Aphena Pharma Solutions - Tennessee, LLC	SULFASALAZINE	500 mg/1	120 TABLET in 1 BOTTLE (71610-706-70)
71610-706-80	71610-706	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET	ORAL	20230516	N/A	NDA AUTHORIZED GENERIC	NDA007073	Aphena Pharma Solutions - Tennessee, LLC	SULFASALAZINE	500 mg/1	180 TABLET in 1 BOTTLE (71610-706-80)
0013-0102-50	0013-0102	HUMAN PRESCRIPTION DRUG	Azulfidine EN-tabs	Sulfasalazine	TABLET, DELAYED RELEASE	ORAL	20200707	N/A	NDA	NDA007073	Pfizer Laboratories Div Pfizer Inc	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (0013-0102-50) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE
0013-0102-60	0013-0102	HUMAN PRESCRIPTION DRUG	Azulfidine EN-tabs	Sulfasalazine	TABLET, DELAYED RELEASE	ORAL	20210215	N/A	NDA	NDA007073	Pfizer Laboratories Div Pfizer Inc	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (0013-0102-60) / 300 TABLET, DELAYED RELEASE in 1 BOTTLE
59762-0104-5	59762-0104	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET, DELAYED RELEASE	ORAL	20200323	N/A	NDA AUTHORIZED GENERIC	NDA007073	Greenstone LLC	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (59762-0104-5) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE
59762-0104-6	59762-0104	HUMAN PRESCRIPTION DRUG	Sulfasalazine	Sulfasalazine	TABLET, DELAYED RELEASE	ORAL	20200406	N/A	NDA AUTHORIZED GENERIC	NDA007073	Greenstone LLC	SULFASALAZINE	500 mg/1	1 BOTTLE in 1 CARTON (59762-0104-6) / 300 TABLET, DELAYED RELEASE in 1 BOTTLE