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
50090-7307-0	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)
50090-7306-2	50090-7306	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 (50090-7306-2)
50090-7306-1	50090-7306	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	60 TABLET, FILM COATED in 1 BOTTLE (50090-7306-1)
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)
68084-269-01	68084-269	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20080903	N/A	ANDA	ANDA040657	American Health Packaging	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-269-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-269-11)
76420-850-05	76420-850	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA040657	Asclemed USA, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76420-850-05)
76420-850-90	76420-850	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA040657	Asclemed USA, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-850-90)
76420-850-30	76420-850	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA040657	Asclemed USA, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-850-30)
76420-850-60	76420-850	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA040657	Asclemed USA, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-850-60)
76420-850-01	76420-850	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA040657	Asclemed USA, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-850-01)
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)
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)
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
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)
55154-2074-0	55154-2074	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20080805	N/A	ANDA	ANDA040657	Cardinal Health 107, LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	10 BLISTER PACK in 1 BAG (55154-2074-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68071-2332-1	68071-2332	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine sulfate	Hydroxychloroquine sulfate	TABLET, FILM COATED	ORAL	20210114	N/A	ANDA	ANDA040657	NuCare Pharmaceuticals,Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-2332-1)
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)