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
68071-4836-7	68071-4836	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20190408	N/A	ANDA	ANDA062269	NuCare Pharmaceuticals,Inc.	DOXYCYCLINE HYCLATE	100 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68071-4836-7)
68071-4836-8	68071-4836	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20190408	N/A	ANDA	ANDA062269	NuCare Pharmaceuticals,Inc.	DOXYCYCLINE HYCLATE	100 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68071-4836-8)
24658-310-05	24658-310	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20250307	N/A	ANDA	ANDA062269	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	DOXYCYCLINE HYCLATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (24658-310-05)
24658-310-07	24658-310	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20250414	N/A	ANDA	ANDA062269	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	DOXYCYCLINE HYCLATE	100 mg/1	300 TABLET, FILM COATED in 1 BOTTLE (24658-310-07)
24658-310-08	24658-310	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20250414	N/A	ANDA	ANDA062269	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	DOXYCYCLINE HYCLATE	100 mg/1	400 TABLET, FILM COATED in 1 BOTTLE (24658-310-08)