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
16571-885-01	16571-885	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	300 mg/1	100 TABLET in 1 BOTTLE (16571-885-01)
16571-885-09	16571-885	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE (16571-885-09)
16571-885-10	16571-885	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	300 mg/1	1000 TABLET in 1 BOTTLE (16571-885-10)
16571-885-50	16571-885	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	300 mg/1	500 TABLET in 1 BOTTLE (16571-885-50)
16571-883-01	16571-883	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (16571-883-01)
16571-883-09	16571-883	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	100 mg/1	90 TABLET in 1 BOTTLE (16571-883-09)
16571-883-10	16571-883	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	100 mg/1	1000 TABLET in 1 BOTTLE (16571-883-10)
16571-883-50	16571-883	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	100 mg/1	500 TABLET in 1 BOTTLE (16571-883-50)
16571-884-01	16571-884	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	200 mg/1	100 TABLET in 1 BOTTLE (16571-884-01)
16571-884-09	16571-884	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	200 mg/1	90 TABLET in 1 BOTTLE (16571-884-09)
16571-884-10	16571-884	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	200 mg/1	1000 TABLET in 1 BOTTLE (16571-884-10)
16571-884-50	16571-884	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20230921	N/A	NDA AUTHORIZED GENERIC	NDA016084	Rising Pharma Holdings, Inc.	ALLOPURINOL	200 mg/1	500 TABLET in 1 BOTTLE (16571-884-50)
67046-1514-3	67046-1514	HUMAN PRESCRIPTION DRUG	Allopurinol	allopurinol	TABLET	ORAL	20250205	N/A	NDA AUTHORIZED GENERIC	NDA016084	Coupler LLC	ALLOPURINOL	300 mg/1	30 TABLET in 1 BLISTER PACK (67046-1514-3)