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=ANDA202214"
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
71335-2585-2 71335-2585 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20250403 N/A ANDA ANDA202214 Bryant Ranch Prepack ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/1; 5 mg/1 60 TABLET in 1 BOTTLE (71335-2585-2)
71335-2585-3 71335-2585 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20250403 N/A ANDA ANDA202214 Bryant Ranch Prepack ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/1; 5 mg/1 90 TABLET in 1 BOTTLE (71335-2585-3)
71335-2585-4 71335-2585 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20250403 N/A ANDA ANDA202214 Bryant Ranch Prepack ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/1; 5 mg/1 8 TABLET in 1 BOTTLE (71335-2585-4)
71335-2585-5 71335-2585 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20250403 N/A ANDA ANDA202214 Bryant Ranch Prepack ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/1; 5 mg/1 20 TABLET in 1 BOTTLE (71335-2585-5)
71335-2740-1 71335-2740 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20250729 N/A ANDA ANDA202214 Bryant Ranch Prepack ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/1; 10 mg/1 1000 TABLET in 1 BOTTLE (71335-2740-1)
71335-2969-1 71335-2969 HUMAN PRESCRIPTION DRUG Hydrocodone Bitartrate and Acetaminophen Hydrocodone Bitartrate and Acetaminophen TABLET ORAL 20251023 N/A ANDA ANDA202214 Bryant Ranch Prepack ACETAMINOPHEN; HYDROCODONE BITARTRATE 325 mg/1; 5 mg/1 100 TABLET in 1 BOTTLE (71335-2969-1)
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