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=ANDA213541"
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
42385-915-90 42385-915 HUMAN PRESCRIPTION DRUG Efavirenz, emtricitabine and tenofovir disoproxil fumarate Efavirenz, emtricitabine and tenofovir disoproxil fumarate TABLET, FILM COATED ORAL 20211222 N/A ANDA ANDA213541 Laurus Labs Limited EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 600 mg/1; 200 mg/1; 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (42385-915-90)
42385-915-30 42385-915 HUMAN PRESCRIPTION DRUG Efavirenz, emtricitabine and tenofovir disoproxil fumarate Efavirenz, emtricitabine and tenofovir disoproxil fumarate TABLET, FILM COATED ORAL 20211222 N/A ANDA ANDA213541 Laurus Labs Limited EFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE 600 mg/1; 200 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42385-915-30)
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