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=ANDA078886"
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
72865-172-25 72865-172 HUMAN PRESCRIPTION DRUG EFAVIRENZ EFAVIRENZ TABLET, FILM COATED ORAL 20210529 N/A ANDA ANDA078886 XLCare Pharmaceuticals Inc. EFAVIRENZ 600 mg/1 250 TABLET, FILM COATED in 1 BOTTLE (72865-172-25)
72865-172-30 72865-172 HUMAN PRESCRIPTION DRUG EFAVIRENZ EFAVIRENZ TABLET, FILM COATED ORAL 20210529 N/A ANDA ANDA078886 XLCare Pharmaceuticals Inc. EFAVIRENZ 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72865-172-30)
31722-504-25 31722-504 HUMAN PRESCRIPTION DRUG Efavirenz Efavirenz TABLET, FILM COATED ORAL 20180427 N/A ANDA ANDA078886 Camber Pharmaceuticals, Inc. EFAVIRENZ 600 mg/1 250 TABLET, FILM COATED in 1 BOTTLE (31722-504-25)
31722-504-30 31722-504 HUMAN PRESCRIPTION DRUG Efavirenz Efavirenz TABLET, FILM COATED ORAL 20180427 N/A ANDA ANDA078886 Camber Pharmaceuticals, Inc. EFAVIRENZ 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-504-30)
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