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=ANDA077859"
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
53002-2645-0 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (53002-2645-0)
53002-2645-1 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 1 TABLET, FILM COATED in 1 BOTTLE (53002-2645-1)
53002-2645-2 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (53002-2645-2)
53002-2645-3 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (53002-2645-3)
53002-2645-4 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (53002-2645-4)
53002-2645-5 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 18 TABLET, FILM COATED in 1 BOTTLE (53002-2645-5)
53002-2645-6 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (53002-2645-6)
53002-2645-9 53002-2645 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220101 N/A ANDA ANDA077859 RPK Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (53002-2645-9)
65862-076-01 65862-076 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20070426 N/A ANDA ANDA077859 Aurobindo Pharma Limited CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-076-01)
72789-330-06 72789-330 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230830 N/A ANDA ANDA077859 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-06)
72789-330-10 72789-330 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230907 N/A ANDA ANDA077859 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-10)
72789-330-14 72789-330 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230814 N/A ANDA ANDA077859 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-14)
72789-330-20 72789-330 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230706 N/A ANDA ANDA077859 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-20)
72789-330-28 72789-330 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20240807 N/A ANDA ANDA077859 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-330-28)
65862-078-01 65862-078 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20070426 N/A ANDA ANDA077859 Aurobindo Pharma Limited CIPROFLOXACIN HYDROCHLORIDE 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-078-01)
65862-078-05 65862-078 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20070426 N/A ANDA ANDA077859 Aurobindo Pharma Limited CIPROFLOXACIN HYDROCHLORIDE 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-078-05)
65862-078-20 65862-078 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20070426 N/A ANDA ANDA077859 Aurobindo Pharma Limited CIPROFLOXACIN HYDROCHLORIDE 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (65862-078-20)
65862-078-50 65862-078 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20070426 N/A ANDA ANDA077859 Aurobindo Pharma Limited CIPROFLOXACIN HYDROCHLORIDE 750 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (65862-078-50)
70934-093-06 70934-093 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20191217 20250131 ANDA ANDA077859 Denton Pharma, Inc. DBA Northwind Pharmaceuticals CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-093-06)
70934-093-14 70934-093 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20191014 20250131 ANDA ANDA077859 Denton Pharma, Inc. DBA Northwind Pharmaceuticals CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-093-14)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase