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
31722-252-01	31722-252	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (31722-252-01)
31722-252-05	31722-252	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	100 mg/1	500 TABLET in 1 BOTTLE (31722-252-05)
31722-252-10	31722-252	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	100 mg/1	1000 TABLET in 1 BOTTLE (31722-252-10)
31722-252-90	31722-252	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	100 mg/1	90 TABLET in 1 BOTTLE (31722-252-90)
31722-253-01	31722-253	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	300 mg/1	100 TABLET in 1 BOTTLE (31722-253-01)
31722-253-05	31722-253	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	300 mg/1	500 TABLET in 1 BOTTLE (31722-253-05)
31722-253-10	31722-253	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	300 mg/1	1000 TABLET in 1 BOTTLE (31722-253-10)
31722-253-90	31722-253	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230803	N/A	ANDA	ANDA217748	Camber Pharmaceuticals, Inc.	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE (31722-253-90)