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
70771-1589-6	70771-1589	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, DELAYED RELEASE	ORAL	20181221	N/A	ANDA	ANDA206772	Zydus Lifesciences Limited	DOXYCYCLINE HYCLATE	150 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1589-6)
70771-1588-5	70771-1588	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, DELAYED RELEASE	ORAL	20181221	N/A	ANDA	ANDA206772	Zydus Lifesciences Limited	DOXYCYCLINE HYCLATE	100 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1588-5)
70771-1588-6	70771-1588	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, DELAYED RELEASE	ORAL	20181221	N/A	ANDA	ANDA206772	Zydus Lifesciences Limited	DOXYCYCLINE HYCLATE	100 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1588-6)
70771-1589-1	70771-1589	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, DELAYED RELEASE	ORAL	20181221	N/A	ANDA	ANDA206772	Zydus Lifesciences Limited	DOXYCYCLINE HYCLATE	150 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1589-1)