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
Article Preview & Download


Go To Issue



Call For Paper

Volume 7 Issue 1

Last Date 25 June 2020


About Us

IJIRT.org enables door in research by providing high quality research articles in open access market.

Send us any query related to your research on editor@ijirt.org

Social Media

Google Verified Reviews

Contact Details

Telephone:+91 820 061 5067
Email: editor@ijirt.org
Website: ijirt.org

Policies