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Stability testing and selection of final packaging for pravastatin tablets

  • At: 2004 FIP Congress in New Orleans (USA)
  • Type: Poster
  • By: LUSINA, Maja (PLIVA - Research Institute Ltd., Analytics, Zagreb, Croatia)
  • Co-author(s): Jurlina (PLIVA - Research Institute Ltd., ZAGREB, Croatia)
    Dumicic (PLIVA - Research Institute Ltd., ZAGREB, Croatia)
    Dragic (PLIVA - Research Institute Ltd., ZAGREB, Croatia)
  • Abstract:

    Within the drug development program of Pravastatin tablets 40 mg, stability testing is performed. It is known that pravastatin is sensitive to a low pH environment and to moisture and will degrade to form its lactone and other degradation products. Since formulation containing basic excipients is patent-protected, other ways of obtaining a..

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Last update 4 October 2019

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