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
50090-6716-0	50090-6716	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231005	N/A	ANDA	ANDA204467	A-S Medication Solutions	ALLOPURINOL	100 mg/1	90 TABLET in 1 BOTTLE (50090-6716-0)
50090-6968-0	50090-6968	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231221	N/A	ANDA	ANDA204467	A-S Medication Solutions	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE (50090-6968-0)
50090-6882-3	50090-6882	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231205	N/A	ANDA	ANDA204467	A-S Medication Solutions	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE (50090-6882-3)
50090-6882-1	50090-6882	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231205	N/A	ANDA	ANDA204467	A-S Medication Solutions	ALLOPURINOL	300 mg/1	30 TABLET in 1 BOTTLE (50090-6882-1)
50090-6882-0	50090-6882	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231205	N/A	ANDA	ANDA204467	A-S Medication Solutions	ALLOPURINOL	300 mg/1	100 TABLET in 1 BOTTLE (50090-6882-0)
71921-240-01	71921-240	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231031	N/A	ANDA	ANDA204467	Florida Pharmaceutical Products, LLC	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (71921-240-01)
71921-242-01	71921-242	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231031	N/A	ANDA	ANDA204467	Florida Pharmaceutical Products, LLC	ALLOPURINOL	300 mg/1	100 TABLET in 1 BOTTLE (71921-242-01)
71921-240-33	71921-240	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231031	N/A	ANDA	ANDA204467	Florida Pharmaceutical Products, LLC	ALLOPURINOL	100 mg/1	30 TABLET in 1 BOTTLE (71921-240-33)
70518-4062-0	70518-4062	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20240504	N/A	ANDA	ANDA204467	REMEDYREPACK INC.	ALLOPURINOL	100 mg/1	30 TABLET in 1 BLISTER PACK (70518-4062-0)
68788-8337-1	68788-8337	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230123	N/A	ANDA	ANDA204467	Preferred Pharmaceuticals Inc.	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (68788-8337-1)
68788-8337-3	68788-8337	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230123	N/A	ANDA	ANDA204467	Preferred Pharmaceuticals Inc.	ALLOPURINOL	100 mg/1	30 TABLET in 1 BOTTLE (68788-8337-3)
68788-8337-6	68788-8337	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230123	N/A	ANDA	ANDA204467	Preferred Pharmaceuticals Inc.	ALLOPURINOL	100 mg/1	60 TABLET in 1 BOTTLE (68788-8337-6)
68788-8337-9	68788-8337	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20230123	N/A	ANDA	ANDA204467	Preferred Pharmaceuticals Inc.	ALLOPURINOL	100 mg/1	90 TABLET in 1 BOTTLE (68788-8337-9)
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)
72189-417-90	72189-417	HUMAN PRESCRIPTION DRUG	ALLOPURINOL	ALLOPURINOL	TABLET	ORAL	20230202	N/A	ANDA	ANDA204467	Direct_Rx	ALLOPURINOL	300 mg/1	90 TABLET in 1 BOTTLE (72189-417-90)
71921-240-50	71921-240	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231031	N/A	ANDA	ANDA204467	Florida Pharmaceutical Products, LLC	ALLOPURINOL	100 mg/1	500 TABLET in 1 BOTTLE (71921-240-50)
16714-576-01	16714-576	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220701	N/A	ANDA	ANDA204467	NorthStar RxLLC	ALLOPURINOL	100 mg/1	30 TABLET in 1 BOTTLE (16714-576-01)
16714-576-02	16714-576	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220701	N/A	ANDA	ANDA204467	NorthStar RxLLC	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (16714-576-02)