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=ANDA209065"
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
83634-600-02 83634-600 HUMAN PRESCRIPTION DRUG Dexmedetomidine dexmedetomidine INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20240315 N/A ANDA ANDA209065 Avenacy Inc. DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 25 VIAL in 1 CARTON (83634-600-02) / 2 mL in 1 VIAL (83634-600-41)
0781-3495-95 0781-3495 HUMAN PRESCRIPTION DRUG DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE INJECTION INTRAVENOUS 20200612 N/A ANDA ANDA209065 Sandoz Inc. DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 10 BOTTLE in 1 CARTON (0781-3495-95) / 100 mL in 1 BOTTLE
71872-7150-1 71872-7150 HUMAN PRESCRIPTION DRUG Dexmedetomidine dexmedetomidine INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20190108 N/A ANDA ANDA209065 Medical Purchasing Solutions, LLC. DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 1 VIAL in 1 BAG (71872-7150-1) / 2 mL in 1 VIAL
0781-3494-95 0781-3494 HUMAN PRESCRIPTION DRUG DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE INJECTION INTRAVENOUS 20200612 N/A ANDA ANDA209065 Sandoz Inc. DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 10 BOTTLE in 1 CARTON (0781-3494-95) / 50 mL in 1 BOTTLE
0781-3493-95 0781-3493 HUMAN PRESCRIPTION DRUG DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE INJECTION INTRAVENOUS 20200612 N/A ANDA ANDA209065 Sandoz Inc. DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 10 VIAL in 1 CARTON (0781-3493-95) / 20 mL in 1 VIAL
70860-605-03 70860-605 HUMAN PRESCRIPTION DRUG Dexmedetomidine dexmedetomidine INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20180301 20240731 ANDA ANDA209065 Athenex Pharmaceutical Division, LLC. DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 25 VIAL in 1 CARTON (70860-605-03) / 2 mL in 1 VIAL (70860-605-41)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase