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
71335-3142-5	71335-3142	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20260608	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	90 TABLET in 1 BOTTLE (71335-3142-5)
71335-3142-6	71335-3142	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20260608	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	120 TABLET in 1 BOTTLE (71335-3142-6)
71335-3142-7	71335-3142	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20260608	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	10 TABLET in 1 BOTTLE (71335-3142-7)
71335-3142-8	71335-3142	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20260608	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	14 TABLET in 1 BOTTLE (71335-3142-8)
71335-3142-9	71335-3142	HUMAN PRESCRIPTION DRUG	HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	TABLET	ORAL	20260608	N/A	ANDA	ANDA040150	Bryant Ranch Prepack	HYDROXYCHLOROQUINE SULFATE	200 mg/1	20 TABLET in 1 BOTTLE (71335-3142-9)