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=ANDA078296"
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
71205-199-60 71205-199 HUMAN PRESCRIPTION DRUG Lovastatin lovastatin TABLET ORAL 20190101 N/A ANDA ANDA078296 Proficient Rx LP LOVASTATIN 40 mg/1 60 TABLET in 1 BOTTLE (71205-199-60)
71205-199-90 71205-199 HUMAN PRESCRIPTION DRUG Lovastatin lovastatin TABLET ORAL 20190101 N/A ANDA ANDA078296 Proficient Rx LP LOVASTATIN 40 mg/1 90 TABLET in 1 BOTTLE (71205-199-90)
0615-8151-39 0615-8151 HUMAN PRESCRIPTION DRUG Lovastatin lovastatin TABLET ORAL 20180709 N/A ANDA ANDA078296 NCS HealthCare of KY, LLC dba Vangard Labs LOVASTATIN 20 mg/1 30 TABLET in 1 BLISTER PACK (0615-8151-39)
0615-8152-39 0615-8152 HUMAN PRESCRIPTION DRUG Lovastatin lovastatin TABLET ORAL 20180710 N/A ANDA ANDA078296 NCS HealthCare of KY, LLC dba Vangard Labs LOVASTATIN 40 mg/1 30 TABLET in 1 BLISTER PACK (0615-8152-39)
68001-314-00 68001-314 HUMAN PRESCRIPTION DRUG Lovastatin lovastatin TABLET ORAL 20170207 N/A ANDA ANDA078296 BluePoint Laboratories LOVASTATIN 10 mg/1 100 TABLET in 1 BOTTLE (68001-314-00)
68001-314-08 68001-314 HUMAN PRESCRIPTION DRUG Lovastatin lovastatin TABLET ORAL 20170207 N/A ANDA ANDA078296 BluePoint Laboratories LOVASTATIN 10 mg/1 1000 TABLET in 1 BOTTLE (68001-314-08)
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