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=ANDA210594"
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
0143-9391-10 0143-9391 HUMAN PRESCRIPTION DRUG REMIFENTANIL HYDROCHLORIDE REMIFENTANIL HYDROCHLORIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20210515 N/A ANDA ANDA210594 Hikma Pharmaceuticals USA Inc. REMIFENTANIL HYDROCHLORIDE 1 mg/mL 10 VIAL in 1 CARTON (0143-9391-10) / 3 mL in 1 VIAL (0143-9391-01)
0143-9392-10 0143-9392 HUMAN PRESCRIPTION DRUG REMIFENTANIL HYDROCHLORIDE REMIFENTANIL HYDROCHLORIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20210515 N/A ANDA ANDA210594 Hikma Pharmaceuticals USA Inc. REMIFENTANIL HYDROCHLORIDE 2 mg/2mL 10 VIAL in 1 CARTON (0143-9392-10) / 5 mL in 1 VIAL (0143-9392-01)
0143-9393-10 0143-9393 HUMAN PRESCRIPTION DRUG REMIFENTANIL HYDROCHLORIDE REMIFENTANIL HYDROCHLORIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION INTRAVENOUS 20210515 N/A ANDA ANDA210594 Hikma Pharmaceuticals USA Inc. REMIFENTANIL HYDROCHLORIDE 5 mg/5mL 10 VIAL in 1 CARTON (0143-9393-10) / 10 mL in 1 VIAL (0143-9393-01)
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