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
68071-2383-4 68071-2383 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210406 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 14 TABLET, COATED in 1 BOTTLE (68071-2383-4)
68071-2383-8 68071-2383 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210406 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 28 TABLET, COATED in 1 BOTTLE (68071-2383-8)
68071-2383-9 68071-2383 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210406 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 90 TABLET, COATED in 1 BOTTLE (68071-2383-9)
68071-2384-1 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 10 TABLET, COATED in 1 BOTTLE (68071-2384-1)
68071-2384-2 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, COATED in 1 BOTTLE (68071-2384-2)
68071-2384-3 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 30 TABLET, COATED in 1 BOTTLE (68071-2384-3)
68071-2384-4 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 14 TABLET, COATED in 1 BOTTLE (68071-2384-4)
68071-2384-5 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 15 TABLET, COATED in 1 BOTTLE (68071-2384-5)
68071-2384-6 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 60 TABLET, COATED in 1 BOTTLE (68071-2384-6)
68071-2384-7 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 21 TABLET, COATED in 1 BOTTLE (68071-2384-7)
68071-2384-8 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 28 TABLET, COATED in 1 BOTTLE (68071-2384-8)
68071-2384-9 68071-2384 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210409 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 90 TABLET, COATED in 1 BOTTLE (68071-2384-9)
68071-2383-1 68071-2383 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210406 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 10 TABLET, COATED in 1 BOTTLE (68071-2383-1)
68071-2383-2 68071-2383 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210406 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 20 TABLET, COATED in 1 BOTTLE (68071-2383-2)
68071-2383-3 68071-2383 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210406 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 30 TABLET, COATED in 1 BOTTLE (68071-2383-3)
51655-490-20 51655-490 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230203 N/A ANDA ANDA208921 Northwind Health Company, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-20)
51655-490-87 51655-490 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20230105 N/A ANDA ANDA208921 Northwind Health Company, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-490-87)
68071-2404-2 68071-2404 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210521 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 2 TABLET, COATED in 1 BOTTLE (68071-2404-2)
68071-2404-4 68071-2404 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210521 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 4 TABLET, COATED in 1 BOTTLE (68071-2404-4)
68071-2404-6 68071-2404 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, COATED ORAL 20210521 N/A ANDA ANDA208921 NuCare Pharmaceuticals,Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET, COATED in 1 BOTTLE (68071-2404-6)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase