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=ANDA201972"
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
71335-1036-8 71335-1036 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20240809 N/A ANDA ANDA201972 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 75 TABLET in 1 BOTTLE (71335-1036-8)
71335-1036-9 71335-1036 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20240809 N/A ANDA ANDA201972 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 100 TABLET in 1 BOTTLE (71335-1036-9)
71335-1036-2 71335-1036 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20240809 N/A ANDA ANDA201972 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 120 TABLET in 1 BOTTLE (71335-1036-2)
71335-1036-3 71335-1036 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20181224 N/A ANDA ANDA201972 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE (71335-1036-3)
71335-1036-4 71335-1036 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20240809 N/A ANDA ANDA201972 Bryant Ranch Prepack ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 28 TABLET in 1 BOTTLE (71335-1036-4)
63187-823-15 63187-823 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20161201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 15 TABLET in 1 BOTTLE (63187-823-15)
63187-823-90 63187-823 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20170301 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 90 TABLET in 1 BOTTLE (63187-823-90)
63187-823-20 63187-823 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20161201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 20 TABLET in 1 BOTTLE (63187-823-20)
63187-823-30 63187-823 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20161201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 30 TABLET in 1 BOTTLE (63187-823-30)
63187-823-60 63187-823 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20161201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 10 mg/1 60 TABLET in 1 BOTTLE (63187-823-60)
63187-984-10 63187-984 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20180201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 10 TABLET in 1 BOTTLE (63187-984-10)
63187-984-60 63187-984 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20180201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 60 TABLET in 1 BOTTLE (63187-984-60)
63187-984-12 63187-984 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20180201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 12 TABLET in 1 BOTTLE (63187-984-12)
63187-984-15 63187-984 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20180201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 15 TABLET in 1 BOTTLE (63187-984-15)
63187-984-30 63187-984 HUMAN PRESCRIPTION DRUG Oxycodone and Acetaminophen Oxycodone and Acetaminophen TABLET ORAL 20180201 N/A ANDA ANDA201972 Proficient Rx LP ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325 mg/1; 5 mg/1 30 TABLET in 1 BOTTLE (63187-984-30)
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