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=ANDA214207"
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
42806-645-01 42806-645 HUMAN PRESCRIPTION DRUG DOXYCYCLINE HYCLATE doxyclycline hyclate TABLET, COATED ORAL 20201216 N/A ANDA ANDA214207 EPIC PHARMA, LLC DOXYCYCLINE HYCLATE 75 mg/1 100 TABLET, COATED in 1 BOTTLE (42806-645-01)
42806-645-05 42806-645 HUMAN PRESCRIPTION DRUG DOXYCYCLINE HYCLATE doxyclycline hyclate TABLET, COATED ORAL 20201216 N/A ANDA ANDA214207 EPIC PHARMA, LLC DOXYCYCLINE HYCLATE 75 mg/1 500 TABLET, COATED in 1 BOTTLE (42806-645-05)
42806-645-60 42806-645 HUMAN PRESCRIPTION DRUG DOXYCYCLINE HYCLATE doxyclycline hyclate TABLET, COATED ORAL 20201216 N/A ANDA ANDA214207 EPIC PHARMA, LLC DOXYCYCLINE HYCLATE 75 mg/1 60 TABLET, COATED in 1 BOTTLE (42806-645-60)
42806-646-01 42806-646 HUMAN PRESCRIPTION DRUG DOXYCYCLINE HYCLATE doxyclycline hyclate TABLET, COATED ORAL 20201216 N/A ANDA ANDA214207 EPIC PHARMA, LLC DOXYCYCLINE HYCLATE 150 mg/1 100 TABLET, COATED in 1 BOTTLE (42806-646-01)
42806-646-05 42806-646 HUMAN PRESCRIPTION DRUG DOXYCYCLINE HYCLATE doxyclycline hyclate TABLET, COATED ORAL 20201216 N/A ANDA ANDA214207 EPIC PHARMA, LLC DOXYCYCLINE HYCLATE 150 mg/1 500 TABLET, COATED in 1 BOTTLE (42806-646-05)
42806-646-60 42806-646 HUMAN PRESCRIPTION DRUG DOXYCYCLINE HYCLATE doxyclycline hyclate TABLET, COATED ORAL 20201216 N/A ANDA ANDA214207 EPIC PHARMA, LLC DOXYCYCLINE HYCLATE 150 mg/1 60 TABLET, COATED in 1 BOTTLE (42806-646-60)
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