DEGRADATION PATHWAY OF PHARMACEUTICAL DOSAGE FORMS

Mahmad Awaiz M. Shaikh; Deepak A. Joshi; Vidyasagar Gali; Shyamlila B. Bavage; Nandkishor B. Bavage

DEGRADATION PATHWAY OF PHARMACEUTICAL DOSAGE FORMS

Authors: Mahmad Awaiz M. Shaikh, Deepak A. Joshi, Vidyasagar Gali, Shyamlila B. Bavage, Nandkishor B. Bavage

Unique Paper ID: 149473
Volume: 6
Issue: 12
PageNo: 517-521

Keywords: No Keywords Found

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)

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Cite This Article

ISSN: 2349-6002
Volume: 6
Issue: 12
PageNo: 517-521

DEGRADATION PATHWAY OF PHARMACEUTICAL DOSAGE FORMS

Available:https://ijirt.org/Article?manuscript=149473

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