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=ANDA070914"
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
0404-9918-01 0404-9918 HUMAN PRESCRIPTION DRUG Nalbuphine Hydrochloride Nalbuphine Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20220113 N/A ANDA ANDA070914 Henry Schein, Inc. NALBUPHINE HYDROCHLORIDE 10 mg/mL 1 AMPULE in 1 BAG (0404-9918-01) / 1 mL in 1 AMPULE
0409-1463-49 0409-1463 HUMAN PRESCRIPTION DRUG Nalbuphine Hydrochloride NALBUPHINE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20080627 N/A ANDA ANDA070914 Hospira, Inc. NALBUPHINE HYDROCHLORIDE 10 mg/mL 10 AMPULE in 1 TRAY (0409-1463-49) / 1 mL in 1 AMPULE (0409-1463-69)
0409-1463-01 0409-1463 HUMAN PRESCRIPTION DRUG Nalbuphine Hydrochloride NALBUPHINE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20050331 N/A ANDA ANDA070914 Hospira, Inc. NALBUPHINE HYDROCHLORIDE 10 mg/mL 10 AMPULE in 1 TRAY (0409-1463-01) / 1 mL in 1 AMPULE (0409-1463-71)
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