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=ANDA079150"
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
16714-695-01 16714-695 HUMAN PRESCRIPTION DRUG Fluconazole Fluconazole POWDER, FOR SUSPENSION ORAL 20090918 N/A ANDA ANDA079150 NorthStar Rx LLC FLUCONAZOLE 10 mg/mL 1 BOTTLE in 1 CARTON (16714-695-01) / 35 mL in 1 BOTTLE
57237-150-35 57237-150 HUMAN PRESCRIPTION DRUG Fluconazole Fluconazole POWDER, FOR SUSPENSION ORAL 20090918 N/A ANDA ANDA079150 Rising Pharma Holdings, Inc. FLUCONAZOLE 40 mg/mL 1 BOTTLE in 1 CARTON (57237-150-35) / 35 mL in 1 BOTTLE
16714-696-01 16714-696 HUMAN PRESCRIPTION DRUG Fluconazole Fluconazole POWDER, FOR SUSPENSION ORAL 20090918 N/A ANDA ANDA079150 NorthStar Rx LLC FLUCONAZOLE 40 mg/mL 1 BOTTLE in 1 CARTON (16714-696-01) / 35 mL in 1 BOTTLE
65862-300-35 65862-300 HUMAN PRESCRIPTION DRUG Fluconazole Fluconazole POWDER, FOR SUSPENSION ORAL 20090918 N/A ANDA ANDA079150 Aurobindo Pharma Limited FLUCONAZOLE 40 mg/mL 1 BOTTLE in 1 CARTON (65862-300-35) / 35 mL in 1 BOTTLE
57237-149-35 57237-149 HUMAN PRESCRIPTION DRUG Fluconazole Fluconazole POWDER, FOR SUSPENSION ORAL 20090918 N/A ANDA ANDA079150 Rising Pharma Holdings, Inc. FLUCONAZOLE 10 mg/mL 1 BOTTLE in 1 CARTON (57237-149-35) / 35 mL in 1 BOTTLE
65862-299-35 65862-299 HUMAN PRESCRIPTION DRUG Fluconazole Fluconazole POWDER, FOR SUSPENSION ORAL 20090918 N/A ANDA ANDA079150 Aurobindo Pharma Limited FLUCONAZOLE 10 mg/mL 1 BOTTLE in 1 CARTON (65862-299-35) / 35 mL in 1 BOTTLE
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