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
63629-9410-1	63629-9410	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20240826	N/A	ANDA	ANDA065285	Bryant Ranch Prepack	DOXYCYCLINE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63629-9410-1)
67296-0989-1	67296-0989	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20051208	N/A	ANDA	ANDA065285	RedPharm Drug	DOXYCYCLINE	50 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67296-0989-1)
67296-0989-2	67296-0989	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20051208	N/A	ANDA	ANDA065285	RedPharm Drug	DOXYCYCLINE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67296-0989-2)
67296-0989-7	67296-0989	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20051208	N/A	ANDA	ANDA065285	RedPharm Drug	DOXYCYCLINE	50 mg/1	28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67296-0989-7)
0527-1537-01	0527-1537	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20080825	N/A	ANDA	ANDA065285	Lannett Company, Inc.	DOXYCYCLINE	150 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-01)
0527-1537-30	0527-1537	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20080825	N/A	ANDA	ANDA065285	Lannett Company, Inc.	DOXYCYCLINE	150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1537-30)
60687-344-25	60687-344	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20171205	N/A	ANDA	ANDA065285	American Health Packaging	DOXYCYCLINE	100 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-344-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-344-95)
0527-1335-01	0527-1335	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20051208	N/A	ANDA	ANDA065285	Lannett Company, Inc.	DOXYCYCLINE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1335-01)
0527-1535-01	0527-1535	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20080825	N/A	ANDA	ANDA065285	Lannett Company, Inc.	DOXYCYCLINE	75 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1535-01)
70934-808-20	70934-808	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20201204	20241231	ANDA	ANDA065285	Denton Pharma, Inc. DBA Northwind Pharmaceuticals	DOXYCYCLINE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-808-20)
0527-1338-25	0527-1338	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20051208	N/A	ANDA	ANDA065285	Lannett Company, Inc.	DOXYCYCLINE	100 mg/1	250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1338-25)
0527-1338-50	0527-1338	HUMAN PRESCRIPTION DRUG	Doxycycline	Doxycycline	TABLET, FILM COATED	ORAL	20051208	N/A	ANDA	ANDA065285	Lannett Company, Inc.	DOXYCYCLINE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1338-50)