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
80425-0319-2	80425-0319	HUMAN PRESCRIPTION DRUG	Doxycycline Monohydrate	Doxycycline Monohydrate	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA209582	Advanced Rx Pharmacy of Tennessee, LLC	DOXYCYCLINE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0319-2)
80425-0319-3	80425-0319	HUMAN PRESCRIPTION DRUG	Doxycycline Monohydrate	Doxycycline Monohydrate	TABLET, FILM COATED	ORAL	20230411	N/A	ANDA	ANDA209582	Advanced Rx Pharmacy of Tennessee, LLC	DOXYCYCLINE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0319-3)
50090-3809-0	50090-3809	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20181112	N/A	ANDA	ANDA209582	A-S Medication Solutions	DOXYCYCLINE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-3809-0)
83008-031-20	83008-031	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20230616	N/A	ANDA	ANDA209582	Quality Care Products, LLC	DOXYCYCLINE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (83008-031-20)