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
72789-519-10 72789-519 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofolxacin TABLET ORAL 20250822 N/A ANDA ANDA208921 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (72789-519-10)
72789-519-12 72789-519 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofolxacin TABLET ORAL 20251024 N/A ANDA ANDA208921 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 12 TABLET in 1 BOTTLE, PLASTIC (72789-519-12)
72789-519-14 72789-519 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofolxacin TABLET ORAL 20250731 N/A ANDA ANDA208921 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 14 TABLET in 1 BOTTLE, PLASTIC (72789-519-14)
72789-519-20 72789-519 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofolxacin TABLET ORAL 20250910 N/A ANDA ANDA208921 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (72789-519-20)
82804-256-06 82804-256 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofolxacin TABLET ORAL 20251218 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 6 TABLET in 1 BOTTLE (82804-256-06)
82804-256-20 82804-256 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofolxacin TABLET ORAL 20251218 N/A ANDA ANDA208921 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 20 TABLET in 1 BOTTLE (82804-256-20)
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