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
70954-805-10	70954-805	HUMAN PRESCRIPTION DRUG	SOVUNA	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20230915	N/A	NDA	NDA214581	ANI Pharmaceuticals, Inc.	HYDROXYCHLOROQUINE SULFATE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70954-805-10)
70954-805-20	70954-805	HUMAN PRESCRIPTION DRUG	SOVUNA	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20230915	N/A	NDA	NDA214581	ANI Pharmaceuticals, Inc.	HYDROXYCHLOROQUINE SULFATE	300 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (70954-805-20)
70954-804-30	70954-804	HUMAN PRESCRIPTION DRUG	SOVUNA	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20230915	N/A	NDA	NDA214581	ANI Pharmaceuticals, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (70954-804-30)
70954-804-20	70954-804	HUMAN PRESCRIPTION DRUG	SOVUNA	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20230915	N/A	NDA	NDA214581	ANI Pharmaceuticals, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70954-804-20)
70954-804-10	70954-804	HUMAN PRESCRIPTION DRUG	SOVUNA	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20230915	N/A	NDA	NDA214581	ANI Pharmaceuticals, Inc.	HYDROXYCHLOROQUINE SULFATE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70954-804-10)