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=ANDA207633"
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
0404-9923-01 0404-9923 HUMAN PRESCRIPTION DRUG NALOXONE HYDROCHLORIDE naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20220113 N/A ANDA ANDA207633 Henry Schein, Inc. NALOXONE HYDROCHLORIDE .4 mg/mL 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9923-01) / 1 mL in 1 VIAL, SINGLE-DOSE
71872-7198-1 71872-7198 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20200129 N/A ANDA ANDA207633 Medical Purchasing Solutions, LLC NALOXONE HYDROCHLORIDE .4 mg/mL 1 VIAL in 1 BAG (71872-7198-1) / 1 mL in 1 VIAL
70069-071-10 70069-071 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20170808 N/A ANDA ANDA207633 Somerset Therapeutics, LLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL in 1 CARTON (70069-071-10) / 1 mL in 1 VIAL (70069-071-01)
50090-5427-0 50090-5427 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20210108 N/A ANDA ANDA207633 A-S Medication Solutions NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL in 1 CARTON (50090-5427-0) / 1 mL in 1 VIAL
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