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=ANDA075079"
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
64380-162-01 64380-162 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride oxybutynin chloride TABLET ORAL 20220930 N/A ANDA ANDA075079 Strides Pharma Science Limited OXYBUTYNIN CHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE, PLASTIC (64380-162-01)
64380-162-02 64380-162 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride oxybutynin chloride TABLET ORAL 20220404 N/A ANDA ANDA075079 Strides Pharma Science Limited OXYBUTYNIN CHLORIDE 5 mg/1 500 TABLET in 1 BOTTLE, PLASTIC (64380-162-02)
64380-162-03 64380-162 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride oxybutynin chloride TABLET ORAL 20220930 N/A ANDA ANDA075079 Strides Pharma Science Limited OXYBUTYNIN CHLORIDE 5 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (64380-162-03)
60687-670-01 60687-670 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride oxybutynin chloride TABLET ORAL 20220720 N/A ANDA ANDA075079 American Health Packaging OXYBUTYNIN CHLORIDE 5 mg/1 100 BLISTER PACK in 1 CARTON (60687-670-01) / 1 TABLET in 1 BLISTER PACK (60687-670-11)
42291-914-50 42291-914 HUMAN PRESCRIPTION DRUG Oxybutynin Chloride oxybutynin chloride TABLET ORAL 20220930 N/A ANDA ANDA075079 AvKARE OXYBUTYNIN CHLORIDE 5 mg/1 500 TABLET in 1 BOTTLE (42291-914-50)
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