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)
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.. The access to the whole abstract and the presentation file is available to FIP members and to congress participants of that specific congress.