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=ANDA040330"
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
63629-2188-1 63629-2188 HUMAN PRESCRIPTION DRUG ENDOCET Oxycodone and Acetaminophen TABLET ORAL 20210312 N/A ANDA ANDA040330 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE (63629-2188-1)
63629-2189-1 63629-2189 HUMAN PRESCRIPTION DRUG ENDOCET Oxycodone and Acetaminophen TABLET ORAL 20210312 N/A ANDA ANDA040330 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 500 TABLET in 1 BOTTLE (63629-2189-1)
63629-2190-1 63629-2190 HUMAN PRESCRIPTION DRUG ENDOCET Oxycodone and Acetaminophen TABLET ORAL 20210312 N/A ANDA ANDA040330 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 7.5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (63629-2190-1)
63629-2187-1 63629-2187 HUMAN PRESCRIPTION DRUG ENDOCET Oxycodone and Acetaminophen TABLET ORAL 20210312 N/A ANDA ANDA040330 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (63629-2187-1)
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