美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=MINOCYCLINE HYDROCHLORIDE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
MINOCYCLINE HYDROCHLORIDE 065436 001 ANDA MINOCYCLINE HYDROCHLORIDE TABLET;ORAL EQ 50MG BASE No No 2007/12/26 2007/12/26 INDICUS PHARMA Prescription
MINOCYCLINE HYDROCHLORIDE 065436 002 ANDA MINOCYCLINE HYDROCHLORIDE TABLET;ORAL EQ 75MG BASE No No 2007/12/26 2007/12/26 INDICUS PHARMA Prescription
MINOCYCLINE HYDROCHLORIDE 065436 003 ANDA MINOCYCLINE HYDROCHLORIDE TABLET;ORAL EQ 100MG BASE No No 2007/12/26 2007/12/26 INDICUS PHARMA Prescription
MINOCYCLINE HYDROCHLORIDE 065470 001 ANDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 50MG BASE No No 2008/03/11 2008/03/11 AUROBINDO PHARMA Prescription
MINOCYCLINE HYDROCHLORIDE 065470 002 ANDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 75MG BASE No No 2008/03/11 2008/03/11 AUROBINDO PHARMA Prescription
MINOCYCLINE HYDROCHLORIDE 065470 003 ANDA MINOCYCLINE HYDROCHLORIDE CAPSULE;ORAL EQ 100MG BASE No No 2008/03/11 2008/03/11 AUROBINDO PHARMA Prescription
MINOCYCLINE HYDROCHLORIDE 090024 001 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 45MG BASE No No 2009/02/03 2009/02/03 IMPAX LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 090024 002 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 90MG BASE No No 2009/02/03 2009/02/03 IMPAX LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 090024 003 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 135MG BASE No No 2009/02/03 2009/02/03 IMPAX LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 065485 001 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 45MG BASE No No 2009/03/17 2009/03/17 BARR LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 065485 002 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 90MG BASE No No 2009/03/17 2009/03/17 BARR LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 065485 003 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 135MG BASE No No 2009/03/17 2009/03/17 BARR LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 065485 004 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 65MG BASE No No 2009/03/17 2012/05/18 BARR LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 065485 005 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 115MG BASE No No 2009/03/17 2012/05/18 BARR LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 065485 007 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 80MG BASE No No 2009/03/17 2017/04/26 BARR LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 065485 008 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 105MG BASE No No 2009/03/17 2017/04/26 BARR LABS INC Discontinued
MINOCYCLINE HYDROCHLORIDE 090422 001 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 45MG BASE No No 2009/08/13 2009/08/13 SANDOZ Prescription
MINOCYCLINE HYDROCHLORIDE 090422 002 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 90MG BASE No No 2009/08/13 2009/08/13 SANDOZ Prescription
MINOCYCLINE HYDROCHLORIDE 090422 003 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL EQ 135MG BASE No No 2009/08/13 2009/08/13 SANDOZ Prescription
MINOCYCLINE HYDROCHLORIDE 090422 004 ANDA MINOCYCLINE HYDROCHLORIDE TABLET, EXTENDED RELEASE; ORAL EQ 65MG BASE No No 2009/08/13 -- SANDOZ None (Tentative Approval)
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