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=ANDA216809"
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
25021-682-20 25021-682 HUMAN PRESCRIPTION DRUG Ketamine Hydrochloride Ketamine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230715 N/A ANDA ANDA216809 Sagent Pharmaceuticals KETAMINE HYDROCHLORIDE 10 mg/mL 10 VIAL in 1 CARTON (25021-682-20) / 20 mL in 1 VIAL
68083-506-10 68083-506 HUMAN PRESCRIPTION DRUG Ketamine Hydrochloride Ketamine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230124 N/A ANDA ANDA216809 Gland Pharma Limited KETAMINE HYDROCHLORIDE 100 mg/mL 10 VIAL in 1 CARTON (68083-506-10) / 5 mL in 1 VIAL
25021-684-05 25021-684 HUMAN PRESCRIPTION DRUG Ketamine Hydrochloride Ketamine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230715 N/A ANDA ANDA216809 Sagent Pharmaceuticals KETAMINE HYDROCHLORIDE 100 mg/mL 10 VIAL in 1 CARTON (25021-684-05) / 5 mL in 1 VIAL
68083-505-10 68083-505 HUMAN PRESCRIPTION DRUG Ketamine Hydrochloride Ketamine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230124 N/A ANDA ANDA216809 Gland Pharma Limited KETAMINE HYDROCHLORIDE 50 mg/mL 10 VIAL in 1 CARTON (68083-505-10) / 10 mL in 1 VIAL
25021-683-10 25021-683 HUMAN PRESCRIPTION DRUG Ketamine Hydrochloride Ketamine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230715 N/A ANDA ANDA216809 Sagent Pharmaceuticals KETAMINE HYDROCHLORIDE 50 mg/mL 10 VIAL in 1 CARTON (25021-683-10) / 10 mL in 1 VIAL
68083-504-10 68083-504 HUMAN PRESCRIPTION DRUG Ketamine Hydrochloride Ketamine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20230124 N/A ANDA ANDA216809 Gland Pharma Limited KETAMINE HYDROCHLORIDE 10 mg/mL 10 VIAL in 1 CARTON (68083-504-10) / 20 mL in 1 VIAL
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