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
68094-047-10	68094-047	HUMAN PRESCRIPTION DRUG	Dexmedetomidine Hydrochloride in Sodium Chloride	Dexmedetomidine Hydrochloride	INJECTION, SOLUTION	INTRAVENOUS	20201123	N/A	ANDA	ANDA212857	Precision Dose, Inc.	DEXMEDETOMIDINE HYDROCHLORIDE	4 ug/mL	10 VIAL in 1 CARTON (68094-047-10) / 20 mL in 1 VIAL (68094-047-01)
68094-147-20	68094-147	HUMAN PRESCRIPTION DRUG	Dexmedetomidine Hydrochloride in Sodium Chloride	Dexmedetomidine Hydrochloride	INJECTION, SOLUTION	INTRAVENOUS	20201123	N/A	ANDA	ANDA212857	Precision Dose, Inc.	DEXMEDETOMIDINE HYDROCHLORIDE	4 ug/mL	20 BOTTLE in 1 CARTON (68094-147-20) / 50 mL in 1 BOTTLE (68094-147-01)
68094-247-10	68094-247	HUMAN PRESCRIPTION DRUG	Dexmedetomidine Hydrochloride in Sodium Chloride	Dexmedetomidine Hydrochloride	INJECTION, SOLUTION	INTRAVENOUS	20201123	N/A	ANDA	ANDA212857	Precision Dose, Inc.	DEXMEDETOMIDINE HYDROCHLORIDE	4 ug/mL	10 BOTTLE in 1 CARTON (68094-247-10) / 100 mL in 1 BOTTLE (68094-247-01)