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=ANDA040608"
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
72887-681-03 72887-681 HUMAN PRESCRIPTION DRUG oxycodone and acetaminophen oxycodone and acetaminophen tablets TABLET ORAL 20200925 N/A ANDA ANDA040608 FH2 Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72887-681-03)
72245-193-03 72245-193 HUMAN PRESCRIPTION DRUG Nalocet oxycodone and acetaminophen TABLET ORAL 20180523 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 2.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72245-193-03)
72245-193-10 72245-193 HUMAN PRESCRIPTION DRUG Nalocet oxycodone and acetaminophen TABLET ORAL 20180523 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 2.5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72245-193-10)
72887-683-03 72887-683 HUMAN PRESCRIPTION DRUG oxycodone and acetaminophen oxycodone and acetaminophen tablets TABLET ORAL 20200925 N/A ANDA ANDA040608 FH2 Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72887-683-03)
72245-682-03 72245-682 HUMAN PRESCRIPTION DRUG Prolate oxycodone and acetaminophen TABLET ORAL 20200217 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 7.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72245-682-03)
72245-682-10 72245-682 HUMAN PRESCRIPTION DRUG Prolate oxycodone and acetaminophen TABLET ORAL 20200217 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 7.5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72245-682-10)
72887-682-03 72887-682 HUMAN PRESCRIPTION DRUG oxycodone and acetaminophen oxycodone and acetaminophen TABLET ORAL 20210302 N/A ANDA ANDA040608 FH2 Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 7.5 mg/1 30 TABLET in 1 BOTTLE (72887-682-03)
72245-681-03 72245-681 HUMAN PRESCRIPTION DRUG Prolate oxycodone and acetaminophen TABLET ORAL 20200217 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72245-681-03)
72245-681-10 72245-681 HUMAN PRESCRIPTION DRUG Prolate oxycodone and acetaminophen TABLET ORAL 20200217 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72245-681-10)
72887-193-03 72887-193 HUMAN PRESCRIPTION DRUG oxycodone and acetaminophen oxycodone and acetaminophen TABLET ORAL 20190603 N/A ANDA ANDA040608 FH2 Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 2.5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72887-193-03)
72245-683-03 72245-683 HUMAN PRESCRIPTION DRUG Prolate oxycodone and acetaminophen TABLET ORAL 20200217 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72245-683-03)
72245-683-10 72245-683 HUMAN PRESCRIPTION DRUG Prolate oxycodone and acetaminophen TABLET ORAL 20200217 N/A ANDA ANDA040608 Forte Bio-Pharma LLC ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 300 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (72245-683-10)
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