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
51862-571-30	51862-571	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, DELAYED RELEASE	ORAL	20201002	N/A	NDA AUTHORIZED GENERIC	NDA050795	Mayne Pharma Commercial LLC	DOXYCYCLINE HYCLATE	80 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-571-30)
51862-558-00	51862-558	HUMAN PRESCRIPTION DRUG	Doryx	doxycycline hyclate	TABLET, DELAYED RELEASE	ORAL	20150413	20250430	NDA	NDA050795	Mayne Pharma Commercial LLC	DOXYCYCLINE HYCLATE	200 mg/1	3 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-558-00)
68308-716-30	68308-716	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, DELAYED RELEASE	ORAL	20171218	N/A	NDA AUTHORIZED GENERIC	NDA050795	Mayne Pharma Commercial LLC	DOXYCYCLINE HYCLATE	200 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-30)
68308-716-60	68308-716	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, DELAYED RELEASE	ORAL	20160201	N/A	NDA AUTHORIZED GENERIC	NDA050795	Mayne Pharma Commercial LLC	DOXYCYCLINE HYCLATE	200 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-60)
51862-560-00	51862-560	HUMAN PRESCRIPTION DRUG	DORYX MPC	doxycycline hyclate	TABLET, DELAYED RELEASE	ORAL	20230102	N/A	NDA	NDA050795	Mayne Pharma Commercial LLC	DOXYCYCLINE HYCLATE	60 mg/1	1 BOTTLE in 1 CARTON (51862-560-00) / 6 TABLET, DELAYED RELEASE in 1 BOTTLE
51862-560-12	51862-560	HUMAN PRESCRIPTION DRUG	DORYX MPC	doxycycline hyclate	TABLET, DELAYED RELEASE	ORAL	20230102	N/A	NDA	NDA050795	Mayne Pharma Commercial LLC	DOXYCYCLINE HYCLATE	60 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-560-12)
51862-560-60	51862-560	HUMAN PRESCRIPTION DRUG	DORYX MPC	doxycycline hyclate	TABLET, DELAYED RELEASE	ORAL	20240513	N/A	NDA	NDA050795	Mayne Pharma Commercial LLC	DOXYCYCLINE HYCLATE	60 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-560-60)