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
63187-419-12	63187-419	HUMAN PRESCRIPTION DRUG	clonidine hydrochloride	clonidine hydrochloride	TABLET	ORAL	20210324	N/A	ANDA	ANDA078895	Proficient Rx LP	CLONIDINE HYDROCHLORIDE	.1 mg/1	12 TABLET in 1 BOTTLE, PLASTIC (63187-419-12)
63187-419-20	63187-419	HUMAN PRESCRIPTION DRUG	clonidine hydrochloride	clonidine hydrochloride	TABLET	ORAL	20190201	N/A	ANDA	ANDA078895	Proficient Rx LP	CLONIDINE HYDROCHLORIDE	.1 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (63187-419-20)
63187-419-30	63187-419	HUMAN PRESCRIPTION DRUG	clonidine hydrochloride	clonidine hydrochloride	TABLET	ORAL	20190201	N/A	ANDA	ANDA078895	Proficient Rx LP	CLONIDINE HYDROCHLORIDE	.1 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63187-419-30)
63187-419-60	63187-419	HUMAN PRESCRIPTION DRUG	clonidine hydrochloride	clonidine hydrochloride	TABLET	ORAL	20190201	N/A	ANDA	ANDA078895	Proficient Rx LP	CLONIDINE HYDROCHLORIDE	.1 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (63187-419-60)
63187-419-90	63187-419	HUMAN PRESCRIPTION DRUG	clonidine hydrochloride	clonidine hydrochloride	TABLET	ORAL	20190201	N/A	ANDA	ANDA078895	Proficient Rx LP	CLONIDINE HYDROCHLORIDE	.1 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (63187-419-90)
29300-135-50	29300-135	HUMAN PRESCRIPTION DRUG	clonidine hydrochloride	clonidine hydrochloride	TABLET	ORAL	20090921	N/A	ANDA	ANDA078895	Unichem Pharmaceuticals (USA), Inc.	CLONIDINE HYDROCHLORIDE	.1 mg/1	5000 TABLET in 1 BOTTLE, PLASTIC (29300-135-50)