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
51655-782-26	51655-782	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220706	N/A	ANDA	ANDA071587	Northwind Pharmaceuticals	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-782-26)
51655-782-52	51655-782	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20210804	N/A	ANDA	ANDA071587	Northwind Pharmaceuticals	ALLOPURINOL	300 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-782-52)
71610-064-45	71610-064	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220421	N/A	ANDA	ANDA071587	Aphena Pharma Solutions - Tennessee, LLC	ALLOPURINOL	300 mg/1	45 TABLET in 1 BOTTLE (71610-064-45)
71610-064-60	71610-064	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20180508	N/A	ANDA	ANDA071587	Aphena Pharma Solutions - Tennessee, LLC	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE (71610-064-60)
70518-3999-0	70518-3999	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20240128	N/A	ANDA	ANDA071587	REMEDYREPACK INC.	ALLOPURINOL	300 mg/1	30 TABLET in 1 BLISTER PACK (70518-3999-0)
55111-730-01	55111-730	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20091001	N/A	ANDA	ANDA071587	Dr. Reddy's Laboratories Limited	ALLOPURINOL	300 mg/1	100 TABLET in 1 BOTTLE (55111-730-01)
55111-730-05	55111-730	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20091001	N/A	ANDA	ANDA071587	Dr. Reddy's Laboratories Limited	ALLOPURINOL	300 mg/1	500 TABLET in 1 BOTTLE (55111-730-05)
55111-730-10	55111-730	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20091001	N/A	ANDA	ANDA071587	Dr. Reddy's Laboratories Limited	ALLOPURINOL	300 mg/1	1000 TABLET in 1 BOTTLE (55111-730-10)