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
71205-636-10 71205-636 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220202 N/A ANDA ANDA077859 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-636-10)
51655-216-20 51655-216 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230628 N/A ANDA ANDA077859 Northwind Pharmaceuticals, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-20)
51655-216-25 51655-216 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230818 N/A ANDA ANDA077859 Northwind Pharmaceuticals, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-25)
51655-216-52 51655-216 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20240110 N/A ANDA ANDA077859 Northwind Pharmaceuticals, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-52)
51655-216-53 51655-216 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230714 N/A ANDA ANDA077859 Northwind Pharmaceuticals, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-53)
51655-216-84 51655-216 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230608 N/A ANDA ANDA077859 Northwind Pharmaceuticals, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-84)
51655-216-87 51655-216 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20230317 N/A ANDA ANDA077859 Northwind Pharmaceuticals, LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-87)
72189-111-20 72189-111 HUMAN PRESCRIPTION DRUG CIPROFLOXACIN ciprofloxacin hydrochloride TABLET, FILM COATED ORAL 20200612 N/A ANDA ANDA077859 DIRECT RX CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)
72189-111-30 72189-111 HUMAN PRESCRIPTION DRUG CIPROFLOXACIN ciprofloxacin hydrochloride TABLET, FILM COATED ORAL 20200612 N/A ANDA ANDA077859 DIRECT RX CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)
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)
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)
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)
70934-093-20 70934-093 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20201106 20250131 ANDA ANDA077859 Denton Pharma, Inc. DBA Northwind Pharmaceuticals CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-093-20)
71205-649-06 71205-649 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220328 N/A ANDA ANDA077859 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (71205-649-06)
71205-649-07 71205-649 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20240626 N/A ANDA ANDA077859 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71205-649-07)
71205-649-10 71205-649 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220328 N/A ANDA ANDA077859 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-649-10)
71205-636-14 71205-636 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin Hydrochloride TABLET, FILM COATED ORAL 20220203 N/A ANDA ANDA077859 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71205-636-14)
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