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=ANDA208921"
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
71205-749-14 71205-749 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230126 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 14 TABLET, COATED in 1 BOTTLE (71205-749-14)
71205-749-20 71205-749 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230126 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 20 TABLET, COATED in 1 BOTTLE (71205-749-20)
71205-749-28 71205-749 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230126 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 28 TABLET, COATED in 1 BOTTLE (71205-749-28)
71205-749-30 71205-749 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230126 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 30 TABLET, COATED in 1 BOTTLE (71205-749-30)
71205-749-60 71205-749 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230126 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 60 TABLET, COATED in 1 BOTTLE (71205-749-60)
71205-749-90 71205-749 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230126 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 90 TABLET, COATED in 1 BOTTLE (71205-749-90)
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