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
27241-108-06	27241-108	HUMAN PRESCRIPTION DRUG	Clonidine hydrochloride	Clonidine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20171121	N/A	ANDA	ANDA209686	Ajanta Pharma USA Inc.	CLONIDINE HYDROCHLORIDE	.1 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-108-06)
60687-462-21	60687-462	HUMAN PRESCRIPTION DRUG	Clonidine hydrochloride	Clonidine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20191217	N/A	ANDA	ANDA209686	American Health Packaging	CLONIDINE HYDROCHLORIDE	.1 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-462-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-462-11)
68001-568-06	68001-568	HUMAN PRESCRIPTION DRUG	Clonidine hydrochloride	Clonidine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230824	N/A	ANDA	ANDA209686	BluePoint Laboratories	CLONIDINE HYDROCHLORIDE	.1 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-568-06)
55700-802-90	55700-802	HUMAN PRESCRIPTION DRUG	Clonidine hydrochloride	Clonidine hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20191011	N/A	ANDA	ANDA209686	Quality Care Products, LLC	CLONIDINE HYDROCHLORIDE	.1 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-802-90)