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=ANDA207135"
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
70756-808-30 70756-808 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL TABLET ORAL 20200501 N/A ANDA ANDA207135 Lifestar Pharma LLC OLMESARTAN MEDOXOMIL 5 mg/1 30 TABLET in 1 BOTTLE (70756-808-30)
70756-808-90 70756-808 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL TABLET ORAL 20200501 N/A ANDA ANDA207135 Lifestar Pharma LLC OLMESARTAN MEDOXOMIL 5 mg/1 90 TABLET in 1 BOTTLE (70756-808-90)
70756-809-30 70756-809 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL TABLET ORAL 20200501 N/A ANDA ANDA207135 Lifestar Pharma LLC OLMESARTAN MEDOXOMIL 20 mg/1 30 TABLET in 1 BOTTLE (70756-809-30)
70756-809-90 70756-809 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL TABLET ORAL 20200501 N/A ANDA ANDA207135 Lifestar Pharma LLC OLMESARTAN MEDOXOMIL 20 mg/1 90 TABLET in 1 BOTTLE (70756-809-90)
70756-810-30 70756-810 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL TABLET ORAL 20200501 N/A ANDA ANDA207135 Lifestar Pharma LLC OLMESARTAN MEDOXOMIL 40 mg/1 30 TABLET in 1 BOTTLE (70756-810-30)
70756-810-90 70756-810 HUMAN PRESCRIPTION DRUG OLMESARTAN MEDOXOMIL OLMESARTAN MEDOXOMIL TABLET ORAL 20200501 N/A ANDA ANDA207135 Lifestar Pharma LLC OLMESARTAN MEDOXOMIL 40 mg/1 90 TABLET in 1 BOTTLE (70756-810-90)
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