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
23155-693-01	23155-693	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20200922	20270930	ANDA	ANDA204467	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (23155-693-01)
23155-693-10	23155-693	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20200922	20290331	ANDA	ANDA204467	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	ALLOPURINOL	100 mg/1	1000 TABLET in 1 BOTTLE (23155-693-10)
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)
71921-242-50	71921-242	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231031	N/A	ANDA	ANDA204467	Florida Pharmaceutical Products, LLC	ALLOPURINOL	300 mg/1	500 TABLET in 1 BOTTLE (71921-242-50)
71921-242-60	71921-242	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20231031	N/A	ANDA	ANDA204467	Florida Pharmaceutical Products, LLC	ALLOPURINOL	300 mg/1	1000 TABLET in 1 BOTTLE (71921-242-60)
68071-3871-1	68071-3871	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20250623	N/A	ANDA	ANDA204467	NuCare Pharmaceuticals,Inc.	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (68071-3871-1)
16714-577-01	16714-577	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220701	N/A	ANDA	ANDA204467	NorthStar RxLLC	ALLOPURINOL	300 mg/1	100 TABLET in 1 BOTTLE (16714-577-01)
16714-577-02	16714-577	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220701	N/A	ANDA	ANDA204467	NorthStar RxLLC	ALLOPURINOL	300 mg/1	500 TABLET in 1 BOTTLE (16714-577-02)
14445-170-00	14445-170	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20160728	N/A	ANDA	ANDA204467	Indoco Remedies Limited	ALLOPURINOL	100 mg/1	1000 TABLET in 1 BOTTLE (14445-170-00)
14445-170-01	14445-170	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20160728	N/A	ANDA	ANDA204467	Indoco Remedies Limited	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (14445-170-01)
14445-170-05	14445-170	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20160728	N/A	ANDA	ANDA204467	Indoco Remedies Limited	ALLOPURINOL	100 mg/1	500 TABLET in 1 BOTTLE (14445-170-05)
71921-241-09	71921-241	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20250522	N/A	ANDA	ANDA204467	Florida Pharmaceutical Products, LLC	ALLOPURINOL	200 mg/1	90 TABLET in 1 BOTTLE (71921-241-09)
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)
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)
50090-6882-3	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)
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)
16714-576-03	16714-576	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220701	N/A	ANDA	ANDA204467	NorthStar RxLLC	ALLOPURINOL	100 mg/1	500 TABLET in 1 BOTTLE (16714-576-03)
16714-576-04	16714-576	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20220701	N/A	ANDA	ANDA204467	NorthStar RxLLC	ALLOPURINOL	100 mg/1	1000 TABLET in 1 BOTTLE (16714-576-04)
71335-2347-1	71335-2347	HUMAN PRESCRIPTION DRUG	Allopurinol	Allopurinol	TABLET	ORAL	20240522	20291031	ANDA	ANDA204467	Bryant Ranch Prepack	ALLOPURINOL	100 mg/1	100 TABLET in 1 BOTTLE (71335-2347-1)