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=ANDA206126"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
51662-1542-1 51662-1542 HUMAN PRESCRIPTION DRUG ETOMIDATE ETOMIDATE INJECTION, SOLUTION INTRAVENOUS 20220409 N/A ANDA ANDA206126 HF Acquisition Co LLC, DBA HealthFirst ETOMIDATE 40 mg/20mL 20 mL in 1 VIAL, SINGLE-DOSE (51662-1542-1)
55150-222-20 55150-222 HUMAN PRESCRIPTION DRUG ETOMIDATE ETOMIDATE INJECTION, SOLUTION INTRAVENOUS 20170224 N/A ANDA ANDA206126 Eugia US LLC ETOMIDATE 40 mg/20mL 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-222-20) / 20 mL in 1 VIAL, SINGLE-DOSE
55150-221-10 55150-221 HUMAN PRESCRIPTION DRUG ETOMIDATE ETOMIDATE INJECTION, SOLUTION INTRAVENOUS 20170224 N/A ANDA ANDA206126 Eugia US LLC ETOMIDATE 20 mg/10mL 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-221-10) / 10 mL in 1 VIAL, SINGLE-DOSE
51662-1634-1 51662-1634 HUMAN PRESCRIPTION DRUG ETOMIDATE injection, solution ETOMIDATE injection, solution INJECTION, SOLUTION INTRAVENOUS 20230925 N/A ANDA ANDA206126 HF Acquisition Co LLC, DBA HealthFirst ETOMIDATE 20 mg/10mL 10 mL in 1 VIAL, SINGLE-DOSE (51662-1634-1)
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