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
23155-693-10	23155-693	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20200922	N/A	ANDA	ANDA204467	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	ALLOPURINOL	100 mg/1	1000 TABLET in 1 BOTTLE (23155-693-10)
51655-945-26	51655-945	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230126	N/A	ANDA	ANDA204467	Northwind Pharmaceuticals, LLC	ALLOPURINOL	100 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-945-26)
51655-945-52	51655-945	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220413	N/A	ANDA	ANDA204467	Northwind Pharmaceuticals, LLC	ALLOPURINOL	100 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-945-52)
68788-8364-1	68788-8364	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230201	N/A	ANDA	ANDA204467	Preferred Pharmaceuticals Inc.	ALLOPURINOL	300 mg/1	100 TABLET in 1 BOTTLE (68788-8364-1)
68788-8364-3	68788-8364	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230201	N/A	ANDA	ANDA204467	Preferred Pharmaceuticals Inc.	ALLOPURINOL	300 mg/1	30 TABLET in 1 BOTTLE (68788-8364-3)
68788-8364-9	68788-8364	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230201	N/A	ANDA	ANDA204467	Preferred Pharmaceuticals Inc.	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE (68788-8364-9)