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
46708-352-31	46708-352	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20200305	N/A	ANDA	ANDA210537	Alembic Pharmaceuticals Limited	DOXYCYCLINE HYCLATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (46708-352-31)
46708-352-60	46708-352	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20200305	N/A	ANDA	ANDA210537	Alembic Pharmaceuticals Limited	DOXYCYCLINE HYCLATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (46708-352-60)
46708-352-91	46708-352	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20200305	N/A	ANDA	ANDA210537	Alembic Pharmaceuticals Limited	DOXYCYCLINE HYCLATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-352-91)
62332-352-31	62332-352	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20200305	N/A	ANDA	ANDA210537	Alembic Pharmaceuticals Inc.	DOXYCYCLINE HYCLATE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62332-352-31)
62332-352-60	62332-352	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20200305	N/A	ANDA	ANDA210537	Alembic Pharmaceuticals Inc.	DOXYCYCLINE HYCLATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62332-352-60)
62332-352-91	62332-352	HUMAN PRESCRIPTION DRUG	Doxycycline Hyclate	Doxycycline Hyclate	TABLET, FILM COATED	ORAL	20200305	N/A	ANDA	ANDA210537	Alembic Pharmaceuticals Inc.	DOXYCYCLINE HYCLATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62332-352-91)