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
70710-1124-3	70710-1124	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180111	N/A	ANDA	ANDA209582	Zydus Pharmaceuticals USA Inc.	DOXYCYCLINE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70710-1124-3)
70710-1122-1	70710-1122	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180111	N/A	ANDA	ANDA209582	Zydus Pharmaceuticals USA Inc.	DOXYCYCLINE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70710-1122-1)
70710-1123-7	70710-1123	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180111	N/A	ANDA	ANDA209582	Zydus Pharmaceuticals USA Inc.	DOXYCYCLINE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (70710-1123-7)
70710-1123-8	70710-1123	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20180111	N/A	ANDA	ANDA209582	Zydus Pharmaceuticals USA Inc.	DOXYCYCLINE	100 mg/1	250 TABLET, FILM COATED in 1 BOTTLE (70710-1123-8)