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=ANDA202801"
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
61919-426-10 61919-426 HUMAN PRESCRIPTION DRUG LEVOFLOXACIN LEVOFLOXACIN TABLET, FILM COATED ORAL 20190424 N/A ANDA ANDA202801 DIRECT RX LEVOFLOXACIN 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (61919-426-10)
72189-338-05 72189-338 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20220321 N/A ANDA ANDA202801 DirectRx LEVOFLOXACIN 750 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (72189-338-05)
72189-338-07 72189-338 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20220321 N/A ANDA ANDA202801 DirectRx LEVOFLOXACIN 750 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (72189-338-07)
72189-338-10 72189-338 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20220321 N/A ANDA ANDA202801 DirectRx LEVOFLOXACIN 750 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (72189-338-10)
72189-338-14 72189-338 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20220321 N/A ANDA ANDA202801 DirectRx LEVOFLOXACIN 750 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (72189-338-14)
70518-0968-0 70518-0968 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20180122 N/A ANDA ANDA202801 REMEDYREPACK INC. LEVOFLOXACIN 750 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0968-0)
70518-0968-3 70518-0968 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20240429 N/A ANDA ANDA202801 REMEDYREPACK INC. LEVOFLOXACIN 750 mg/1 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0968-3)
50090-3214-1 50090-3214 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20150109 N/A ANDA ANDA202801 A-S Medication Solutions LEVOFLOXACIN 750 mg/1 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3214-1)
50090-3214-2 50090-3214 HUMAN PRESCRIPTION DRUG Levofloxacin Levofloxacin TABLET, FILM COATED ORAL 20150109 N/A ANDA ANDA202801 A-S Medication Solutions LEVOFLOXACIN 750 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3214-2)
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