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Stability indicating method for the determination of venlafaxine impurities and degradation products in venlafaxine hydrochloride sustained release tablets

  • At: 2010 FIP Congress in Lisbon (Portugal)
  • Type: Poster
  • By: GAMPA, Vijaykumar (Vikas institute of pharmaceutical sciences,rajahmundry, East Godavari, India)
  • Co-author(s): t.V, Narayana (SBD COLLEGE OF PHARMACY, BANGALORE, India)
    Cs, Srinivas (STRETHCLIDEARCOLABS, BANGALORE, India)
  • Abstract:

    Abstract

    The HPLC method is described for the determination of venlafaxine impurities and degradation products in a pharmaceutical dosage form. The analyte is contained in a placebo matrix with sustained release form and with a high amount of non-soluble excipients, some of which can interfere with the analysis. This makes their separation and..

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Last update 4 October 2019

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