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DEVELOPMENT OF DISSOLUTION TEST FOR DRONEDARONE HYDROCHLORIDE PHARMACEUTICAL FORMULATION

  • Unique Paper ID: 153089
  • Volume: 8
  • Issue: 5
  • PageNo: 431-435
  • Abstract:
  • Formulation quality control aspects are mainly deals with evaluation of dissolution and drug release profile of drugs from various dosage forms. In this study a RP-HPLC method was developed and validated for the dissolution study of Dronedarone Hydrochloride from tablet formulation. The validated method was applied for any other formulation due to its acceptability as per the ICH guidelines. The various validation parameters pass the acceptance criteria as per the ICH guidelines.
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Cite This Article

  • ISSN: 2349-6002
  • Volume: 8
  • Issue: 5
  • PageNo: 431-435

DEVELOPMENT OF DISSOLUTION TEST FOR DRONEDARONE HYDROCHLORIDE PHARMACEUTICAL FORMULATION

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