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)
检索条件:" 注册申请号=ANDA204023"
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
71872-7030-1 71872-7030 HUMAN PRESCRIPTION DRUG Dexmedetomidine hydrochloride Dexmedetomidine hydrochloride INJECTION, SOLUTION INTRAVENOUS 20200228 N/A ANDA ANDA204023 Medical Purchasing Solutions, LLC DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 1 VIAL in 1 BAG (71872-7030-1) / 2 mL in 1 VIAL
16729-239-93 16729-239 HUMAN PRESCRIPTION DRUG Dexmedetomidine Dexmedetomidine INJECTION, SOLUTION INTRAVENOUS 20161221 N/A ANDA ANDA204023 Accord Healthcare Inc. DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 25 VIAL in 1 CARTON (16729-239-93) / 2 mL in 1 VIAL (16729-239-30)
16729-432-93 16729-432 HUMAN PRESCRIPTION DRUG DEXMEDETOMIDINE DEXMEDETOMIDINE INJECTION, SOLUTION INTRAVENOUS 20180831 N/A ANDA ANDA204023 Accord Healthcare Inc. DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 25 VIAL in 1 CARTON (16729-432-93) / 2 mL in 1 VIAL (16729-432-30)
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