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=ANDA210664"
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
42192-501-05 42192-501 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline hyclate TABLET, COATED ORAL 20200821 N/A ANDA ANDA210664 Acella Pharmaceuticals, LLC DOXYCYCLINE HYCLATE 100 mg/1 500 TABLET, COATED in 1 BOTTLE (42192-501-05)
42192-501-50 42192-501 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline hyclate TABLET, COATED ORAL 20200821 N/A ANDA ANDA210664 Acella Pharmaceuticals, LLC DOXYCYCLINE HYCLATE 100 mg/1 50 TABLET, COATED in 1 BOTTLE (42192-501-50)
70518-3363-0 70518-3363 HUMAN PRESCRIPTION DRUG Doxycycline Doxycycline hyclate TABLET, COATED ORAL 20220210 N/A ANDA ANDA210664 REMEDYREPACK INC. DOXYCYCLINE HYCLATE 100 mg/1 14 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3363-0)
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