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=ANDA210321"
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
55150-297-10 55150-297 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride INJECTION, SOLUTION INTRAVENOUS 20201207 N/A ANDA ANDA210321 Eugia US LLC DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 10 POUCH in 1 CARTON (55150-297-10) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
55150-296-10 55150-296 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride INJECTION, SOLUTION INTRAVENOUS 20201207 N/A ANDA ANDA210321 Eugia US LLC DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 10 POUCH in 1 CARTON (55150-296-10) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
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