DEGRADATION PATHWAY OF PHARMACEUTICAL DOSAGE FORMS

DEGRADATION PATHWAY OF PHARMACEUTICAL DOSAGE FORMS
Author(s):
Mahmad Awaiz M. Shaikh, Deepak A. Joshi, Vidyasagar Gali, Shyamlila B. Bavage, Nandkishor B. Bavage
Keywords:

Abstract
In the formulation of drug dosage forms, stability consideration for the active pharmaceutical ingredients (API) and the excipients is critical. This is because degradation process leads to loss of efficacy, making the drug in a specific packaging not to remain in the specified chemical, physical, microbiological, therapeutic and toxicological specifications. Guillory and Poust (2002), Barnes (2013).Therefore, understanding the degradation pathways in order to achieve stability of both the drug substance and drug products is a key quality goal. Porter (2013)
Article Details
Unique Paper ID: 149473 Publication Volume & Issue: Volume 6, Issue 12 Page(s): 517 - 521
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