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
71335-0897-9	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0897-9)
68071-2912-2	68071-2912	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20230125	N/A	ANDA	ANDA040657	NuCare Pharmaceuticals,Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (68071-2912-2)
68071-2912-3	68071-2912	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20230125	N/A	ANDA	ANDA040657	NuCare Pharmaceuticals,Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2912-3)
68071-2912-9	68071-2912	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20230111	N/A	ANDA	ANDA040657	NuCare Pharmaceuticals,Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2912-9)
82009-045-05	82009-045	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20220930	N/A	ANDA	ANDA040657	Quallent Pharmaceuticals Health LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-045-05)
68382-096-01	68382-096	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20080103	N/A	ANDA	ANDA040657	Zydus Pharmaceuticals USA Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-096-01)
68382-096-05	68382-096	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20080103	N/A	ANDA	ANDA040657	Zydus Pharmaceuticals USA Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-096-05)
68382-096-77	68382-096	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20080103	N/A	ANDA	ANDA040657	Zydus Pharmaceuticals USA Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 BLISTER PACK in 1 CARTON (68382-096-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-096-30)
71610-506-30	71610-506	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20201222	N/A	ANDA	ANDA040657	Aphena Pharma Solutions - Tennessee, LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71610-506-30)
71610-506-53	71610-506	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20201222	N/A	ANDA	ANDA040657	Aphena Pharma Solutions - Tennessee, LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-506-53)
68788-7747-2	68788-7747	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20200701	N/A	ANDA	ANDA040657	Preferred Pharmaceuticals, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-7747-2)
68788-7747-3	68788-7747	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20200701	N/A	ANDA	ANDA040657	Preferred Pharmaceuticals, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7747-3)
68071-4648-1	68071-4648	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20181204	N/A	ANDA	ANDA040657	NuCare Pharmaceuticals,Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-4648-1)
63739-777-10	63739-777	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA040657	McKesson Corporation dba SKY Packaging	HYDROXYCHLOROQUINE SULFATE	200 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-777-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK