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=ANDA062059"
符合检索条件的记录共 6 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
62135-776-38 62135-776 HUMAN PRESCRIPTION DRUG AMOXICILLIN Amoxicillin POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA062059 Chartwell RX, LLC AMOXICILLIN 125 mg/5mL 150 mL in 1 BOTTLE (62135-776-38)
62135-776-42 62135-776 HUMAN PRESCRIPTION DRUG AMOXICILLIN Amoxicillin POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA062059 Chartwell RX, LLC AMOXICILLIN 125 mg/5mL 100 mL in 1 BOTTLE (62135-776-42)
62135-776-68 62135-776 HUMAN PRESCRIPTION DRUG AMOXICILLIN Amoxicillin POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA062059 Chartwell RX, LLC AMOXICILLIN 125 mg/5mL 80 mL in 1 BOTTLE (62135-776-68)
62135-777-68 62135-777 HUMAN PRESCRIPTION DRUG AMOXICILLIN Amoxicillin POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA062059 Chartwell RX, LLC AMOXICILLIN 250 mg/5mL 80 mL in 1 BOTTLE (62135-777-68)
62135-777-42 62135-777 HUMAN PRESCRIPTION DRUG AMOXICILLIN Amoxicillin POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA062059 Chartwell RX, LLC AMOXICILLIN 250 mg/5mL 100 mL in 1 BOTTLE (62135-777-42)
62135-777-38 62135-777 HUMAN PRESCRIPTION DRUG AMOXICILLIN Amoxicillin POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA062059 Chartwell RX, LLC AMOXICILLIN 250 mg/5mL 150 mL in 1 BOTTLE (62135-777-38)
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