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
71335-0897-3	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20180706	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0897-3)
71335-0897-4	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20180710	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-0897-4)
71335-0897-5	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20190225	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0897-5)
71335-0897-6	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0897-6)
71335-0897-7	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-0897-7)
71335-0897-8	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0897-8)
71335-0897-9	71335-0897	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA040657	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0897-9)
65841-633-01	65841-633	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20080103	N/A	ANDA	ANDA040657	Zydus Lifesciences Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-633-01)
65841-633-05	65841-633	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20080103	N/A	ANDA	ANDA040657	Zydus Lifesciences Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-633-05)
65841-633-30	65841-633	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20080103	N/A	ANDA	ANDA040657	Zydus Lifesciences Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	10 BLISTER PACK in 1 CARTON (65841-633-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
50090-7307-0	50090-7307	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20241014	N/A	ANDA	ANDA040657	A-S Medication Solutions	HYDROXYCHLOROQUINE SULFATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-7307-0)
16714-110-01	16714-110	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20191001	N/A	ANDA	ANDA040657	Northstar Rx LLC.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-110-01)
16714-110-02	16714-110	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20211203	N/A	ANDA	ANDA040657	Northstar Rx LLC.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16714-110-02)
50090-6629-0	50090-6629	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20230825	N/A	ANDA	ANDA040657	A-S Medication Solutions	HYDROXYCHLOROQUINE SULFATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6629-0)
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)