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=ANDA040105"
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
63187-406-15 63187-406 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone hydrochloride and Acetaminophen TABLET ORAL 20190101 N/A ANDA ANDA040105 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 15 TABLET in 1 BOTTLE, PLASTIC (63187-406-15)
63187-406-20 63187-406 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone hydrochloride and Acetaminophen TABLET ORAL 20190101 N/A ANDA ANDA040105 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (63187-406-20)
63187-406-30 63187-406 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone hydrochloride and Acetaminophen TABLET ORAL 20190101 N/A ANDA ANDA040105 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (63187-406-30)
63187-406-60 63187-406 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone hydrochloride and Acetaminophen TABLET ORAL 20190101 N/A ANDA ANDA040105 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (63187-406-60)
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