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=ANDA076639"
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
0904-7243-95 0904-7243 HUMAN PRESCRIPTION DRUG ciprofloxacin ciprofloxacin TABLET, FILM COATED ORAL 20220823 N/A ANDA ANDA076639 Major Pharmaceuticals CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (0904-7243-95)
55154-0193-0 55154-0193 HUMAN PRESCRIPTION DRUG ciprofloxacin ciprofloxacin TABLET, FILM COATED ORAL 20251017 N/A ANDA ANDA076639 Cardinal Health 107, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 10 BLISTER PACK in 1 BAG (55154-0193-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
43063-869-06 43063-869 HUMAN PRESCRIPTION DRUG ciprofloxacin ciprofloxacin TABLET ORAL 20180804 N/A ANDA ANDA076639 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET in 1 BOTTLE, PLASTIC (43063-869-06)
43063-869-08 43063-869 HUMAN PRESCRIPTION DRUG ciprofloxacin ciprofloxacin TABLET ORAL 20180711 N/A ANDA ANDA076639 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 8 TABLET in 1 BOTTLE, PLASTIC (43063-869-08)
43063-869-10 43063-869 HUMAN PRESCRIPTION DRUG ciprofloxacin ciprofloxacin TABLET ORAL 20180822 N/A ANDA ANDA076639 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (43063-869-10)
43063-869-20 43063-869 HUMAN PRESCRIPTION DRUG ciprofloxacin ciprofloxacin TABLET ORAL 20180817 N/A ANDA ANDA076639 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (43063-869-20)
43063-869-30 43063-869 HUMAN PRESCRIPTION DRUG ciprofloxacin ciprofloxacin TABLET ORAL 20180817 N/A ANDA ANDA076639 PD-Rx Pharmaceuticals, Inc. CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-869-30)
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