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=ANDA070918"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0404-9917-10 0404-9917 HUMAN PRESCRIPTION DRUG Nalbuphine Hydrochloride nalbuphine hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20220113 N/A ANDA ANDA070918 Henry Schein, Inc. NALBUPHINE HYDROCHLORIDE 20 mg/mL 1 VIAL, MULTI-DOSE in 1 BAG (0404-9917-10) / 10 mL in 1 VIAL, MULTI-DOSE
51662-1418-1 51662-1418 HUMAN PRESCRIPTION DRUG NALBUPHINE HCI NALBUPHINE HCI INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20191029 N/A ANDA ANDA070918 HF Acquisition Co LLC, DBA HealthFirst NALBUPHINE HYDROCHLORIDE 20 mg/mL 1 VIAL, MULTI-DOSE in 1 CARTON (51662-1418-1) / 10 mL in 1 VIAL, MULTI-DOSE
0409-1467-01 0409-1467 HUMAN PRESCRIPTION DRUG Nalbuphine Hydrochloride NALBUPHINE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20050516 N/A ANDA ANDA070918 Hospira, Inc. NALBUPHINE HYDROCHLORIDE 20 mg/mL 25 CARTON in 1 CASE (0409-1467-01) / 1 VIAL, MULTI-DOSE in 1 CARTON (0409-1467-61) / 10 mL in 1 VIAL, MULTI-DOSE
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