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
69238-1544-5	69238-1544	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20190917	N/A	ANDA	ANDA210577	Amneal Pharmaceuticals NY LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69238-1544-5)
69238-1544-1	69238-1544	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20180517	N/A	ANDA	ANDA210577	Amneal Pharmaceuticals NY LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69238-1544-1)
60219-1544-1	60219-1544	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20180517	N/A	ANDA	ANDA210577	Amneal Pharmaceuticals NY LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60219-1544-1)
50090-4659-1	50090-4659	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20191028	N/A	ANDA	ANDA210577	A-S Medication Solutions	HYDROXYCHLOROQUINE SULFATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-4659-1)
50090-4659-2	50090-4659	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20191028	N/A	ANDA	ANDA210577	A-S Medication Solutions	HYDROXYCHLOROQUINE SULFATE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-4659-2)
50090-4659-3	50090-4659	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20200317	N/A	ANDA	ANDA210577	A-S Medication Solutions	HYDROXYCHLOROQUINE SULFATE	200 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (50090-4659-3)