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
67046-1523-3	67046-1523	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20250224	N/A	ANDA	ANDA040766	Coupler LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1523-3)
83980-001-01	83980-001	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20240603	N/A	ANDA	ANDA040766	Ipca Laboratories Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (83980-001-01)
83980-001-05	83980-001	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20240603	N/A	ANDA	ANDA040766	Ipca Laboratories Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (83980-001-05)
83980-001-10	83980-001	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20240603	N/A	ANDA	ANDA040766	Ipca Laboratories Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (83980-001-10)
83980-001-97	83980-001	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20240603	N/A	ANDA	ANDA040766	Ipca Laboratories Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (83980-001-97)