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=ANDA206837"
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
65862-891-01 65862-891 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-891-01)
65862-891-03 65862-891 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 50 mg/1 3 BLISTER PACK in 1 CARTON (65862-891-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-891-10)
65862-891-05 65862-891 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-891-05)
65862-891-30 65862-891 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-891-30)
65862-892-01 65862-892 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-892-01)
65862-892-03 65862-892 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 200 mg/1 3 BLISTER PACK in 1 CARTON (65862-892-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-892-10)
65862-892-05 65862-892 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-892-05)
65862-892-30 65862-892 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 Aurobindo Pharma Limited VORICONAZOLE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-892-30)
16714-198-01 16714-198 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 NorthStar Rx LLC VORICONAZOLE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-198-01)
16714-199-01 16714-199 HUMAN PRESCRIPTION DRUG Voriconazole Voriconazole TABLET, FILM COATED ORAL 20160122 N/A ANDA ANDA206837 NorthStar Rx LLC VORICONAZOLE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (16714-199-01)
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