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=ANDA212455"
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
55150-327-10 55150-327 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20191015 N/A ANDA ANDA212455 Eugia US LLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-327-10) / 1 mL in 1 VIAL, SINGLE-DOSE
55150-327-25 55150-327 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20191015 N/A ANDA ANDA212455 Eugia US LLC NALOXONE HYDROCHLORIDE .4 mg/mL 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-327-25) / 1 mL in 1 VIAL, SINGLE-DOSE
51662-1544-1 51662-1544 HUMAN PRESCRIPTION DRUG NALOXONE HYDROCHLORIDE NALOXONE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20210808 N/A ANDA ANDA212455 HF Acquisition Co LLC, DBA HealthFirst NALOXONE HYDROCHLORIDE .4 mg/mL 1 mL in 1 VIAL, SINGLE-DOSE (51662-1544-1)
51662-1544-3 51662-1544 HUMAN PRESCRIPTION DRUG NALOXONE HYDROCHLORIDE NALOXONE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20220422 N/A ANDA ANDA212455 HF Acquisition Co LLC, DBA HealthFirst NALOXONE HYDROCHLORIDE .4 mg/mL 10 POUCH in 1 CASE (51662-1544-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1544-2) / 1 mL in 1 VIAL, SINGLE-DOSE
71872-7219-1 71872-7219 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20200911 N/A ANDA ANDA212455 Medical Purchasing Solutions, LLC NALOXONE HYDROCHLORIDE .4 mg/mL 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7219-1) / 1 mL in 1 VIAL, SINGLE-DOSE
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