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=ANDA202142"
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
72245-648-12 72245-648 HUMAN PRESCRIPTION DRUG Prolate oxycodone hydrochloride and acetaminophen SOLUTION ORAL 20200301 N/A ANDA ANDA202142 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/5mL; 10 mg/5mL 120 mL in 1 BOTTLE, PLASTIC (72245-648-12)
72245-648-50 72245-648 HUMAN PRESCRIPTION DRUG Prolate oxycodone hydrochloride and acetaminophen SOLUTION ORAL 20200301 N/A ANDA ANDA202142 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/5mL; 10 mg/5mL 500 mL in 1 BOTTLE, PLASTIC (72245-648-50)
72887-648-12 72887-648 HUMAN PRESCRIPTION DRUG oxycodone hydrochloride and acetaminophen oxycodone hydrochloride and acetaminophen SOLUTION ORAL 20200301 N/A ANDA ANDA202142 FH2 Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/5mL; 10 mg/5mL 120 mL in 1 BOTTLE, PLASTIC (72887-648-12)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase