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
42385-927-01	42385-927	HUMAN PRESCRIPTION DRUG	Hydroxychloroquine Sulfate	Hydroxychloroquine Sulfate	TABLET, FILM COATED	ORAL	20190905	20250228	ANDA	ANDA210959	Laurus Labs Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42385-927-01)
42385-971-05	42385-971	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	HYDROXYCHLOROQUINE SULFATE	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA210959	Laurus Labs Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42385-971-05)
42385-971-01	42385-971	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	HYDROXYCHLOROQUINE SULFATE	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA210959	Laurus Labs Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42385-971-01)
42385-971-11	42385-971	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	HYDROXYCHLOROQUINE SULFATE	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA210959	Laurus Labs Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42385-971-11)
42385-971-60	42385-971	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	HYDROXYCHLOROQUINE SULFATE	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA210959	Laurus Labs Limited	HYDROXYCHLOROQUINE SULFATE	200 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (42385-971-60)