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=ANDA207956"
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
79672-613-50 79672-613 HUMAN PRESCRIPTION DRUG Sodium Chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20210215 N/A ANDA ANDA207956 Nextgen Pharmaceuticals LLC SODIUM CHLORIDE 9 g/1000mL 10 BAG in 1 CARTON (79672-613-50) / 1000 mL in 1 BAG (79672-613-05)
79672-613-30 79672-613 HUMAN PRESCRIPTION DRUG Sodium Chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20210215 N/A ANDA ANDA207956 Nextgen Pharmaceuticals LLC SODIUM CHLORIDE 9 g/1000mL 28 BAG in 1 CARTON (79672-613-30) / 250 mL in 1 BAG (79672-613-03)
79672-613-20 79672-613 HUMAN PRESCRIPTION DRUG Sodium Chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20210215 N/A ANDA ANDA207956 Nextgen Pharmaceuticals LLC SODIUM CHLORIDE 9 g/1000mL 70 BAG in 1 CARTON (79672-613-20) / 100 mL in 1 BAG (79672-613-02)
79672-613-10 79672-613 HUMAN PRESCRIPTION DRUG Sodium Chloride SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20210215 N/A ANDA ANDA207956 Nextgen Pharmaceuticals LLC SODIUM CHLORIDE 9 g/1000mL 115 BAG in 1 CARTON (79672-613-10) / 50 mL in 1 BAG (79672-613-01)
51662-1609-1 51662-1609 HUMAN PRESCRIPTION DRUG 0.9% SODIUM CHLORIDE 0.9% SODIUM CHLORIDE INJECTION, SOLUTION INTRAVENOUS 20220731 N/A ANDA ANDA207956 HF Acquisition Co LLC, DBA HealthFirst SODIUM CHLORIDE 9 g/1000mL 500 mL in 1 BAG (51662-1609-1)
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