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=ANDA209058"
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
68083-234-10 68083-234 HUMAN PRESCRIPTION DRUG Etomidate Etomidate Injection SOLUTION INTRAVENOUS 20170520 N/A ANDA ANDA209058 Gland Pharma Limited ETOMIDATE 2 mg/mL 10 VIAL in 1 CARTON (68083-234-10) / 10 mL in 1 VIAL (68083-234-01)
68083-235-10 68083-235 HUMAN PRESCRIPTION DRUG Etomidate Etomidate Injection SOLUTION INTRAVENOUS 20170520 N/A ANDA ANDA209058 Gland Pharma Limited ETOMIDATE 2 mg/mL 10 VIAL in 1 CARTON (68083-235-10) / 20 mL in 1 VIAL (68083-235-01)
72266-147-10 72266-147 HUMAN PRESCRIPTION DRUG Etomidate Etomidate Injection SOLUTION INTRAVENOUS 20190903 N/A ANDA ANDA209058 Fosun Pharma USA Inc ETOMIDATE 2 mg/mL 10 VIAL in 1 CARTON (72266-147-10) / 20 mL in 1 VIAL (72266-147-01)
72266-146-10 72266-146 HUMAN PRESCRIPTION DRUG Etomidate Etomidate Injection SOLUTION INTRAVENOUS 20190903 N/A ANDA ANDA209058 Fosun Pharma USA Inc ETOMIDATE 2 mg/mL 10 VIAL in 1 CARTON (72266-146-10) / 10 mL in 1 VIAL (72266-146-01)
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