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
71335-2813-1	71335-2813	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20251002	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET in 1 BOTTLE (71335-2813-1)
82619-131-01	82619-131	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20250508	N/A	ANDA	ANDA040150	Creekwood Pharmaceuticals LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET in 1 BOTTLE (82619-131-01)
82619-131-02	82619-131	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20250508	N/A	ANDA	ANDA040150	Creekwood Pharmaceuticals LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET in 1 BOTTLE (82619-131-02)
82619-131-03	82619-131	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20250508	N/A	ANDA	ANDA040150	Creekwood Pharmaceuticals LLC	HYDROXYCHLOROQUINE SULFATE	200 mg/1	1000 TABLET in 1 BOTTLE (82619-131-03)
72162-2467-1	72162-2467	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20250715	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	100 TABLET in 1 BOTTLE (72162-2467-1)
72162-2467-5	72162-2467	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20250715	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET in 1 BOTTLE (72162-2467-5)
71335-2814-1	71335-2814	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20251002	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	500 TABLET in 1 BOTTLE (71335-2814-1)