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=ANDA201618"
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
55111-731-30 55111-731 HUMAN PRESCRIPTION DRUG Valsartan Valsartan TABLET, FILM COATED ORAL 20211005 N/A ANDA ANDA201618 Dr. Reddy's Laboratories Limited VALSARTAN 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55111-731-30)
55111-731-05 55111-731 HUMAN PRESCRIPTION DRUG Valsartan Valsartan TABLET, FILM COATED ORAL 20211005 N/A ANDA ANDA201618 Dr. Reddy's Laboratories Limited VALSARTAN 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (55111-731-05)
55111-731-01 55111-731 HUMAN PRESCRIPTION DRUG Valsartan Valsartan TABLET, FILM COATED ORAL 20211005 N/A ANDA ANDA201618 Dr. Reddy's Laboratories Limited VALSARTAN 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (55111-731-01)
67046-1142-3 67046-1142 HUMAN PRESCRIPTION DRUG Valsartan Valsartan TABLET, FILM COATED ORAL 20241108 N/A ANDA ANDA201618 Coupler LLC VALSARTAN 80 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1142-3)
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