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A Quality Control Study of Different Brands of Clopidogrel Tablets
Published in June 2022 Issue 3 (Vol. 12, Issue 3, 2022)

Abstract
Clopidogrel is an orally administered medicine that lowers the risk of heart disease. The production process is defined by drug quality, and every pharmaceutical business aims for it, although it is often difficult to attain. The purpose of this study was to look at the quality control parameters of several commercially available Clopidogrel tablets. Four distinct marketed brands of Clopidogrel 75 mg tablets available in the Mangalore market were collected from different pharmacies in Mangalore city to examine the quality. Weight variation, hardness, thickness, and friability, among other quality indicators, were determined according to established protocols. Then there was the in-vitro dissolution test, potency, and disintegration time. All of the brands met the requirements of the Pharmacopoeia since they had a weight fluctuation range that was acceptable. All brands were less than 1% friable, and there were no significant differences in disintegration times, since they all dissolved within 15 minutes. In terms of dissolution profile, all brands had an acceptable dissolving time, releasing more than 60% of the drug in less than 45 minutes. All brands’ hardness fell inside the range. All of the brands also meet the potency requirements. This investigation found that the majority of commercially available Clopidogrel pills in Mangalore are of good quality and meet pharmacopoeia requirements.
Authors (6)
Baiju Mathews
View all publications →Abdul Razik
View all publications →Faris KT
View all publications →Harsha Dinesh
View all publications →M. Hashim
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Article Information
Published in:
June 2022 Issue 3 (Vol. 12, Issue 3, 2022)- Article ID:
- AJPTR123012
- Paper ID:
- AJPTR-01-000104
- Published Date:
- 2022-06-01
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Downloads:1,273
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How to Cite
Mathews & Razik & KT & Dinesh & Hashim & Sujaya (2022). A Quality Control Study of Different Brands of Clopidogrel Tablets. American Journal of PharmTech Research, 12(3), xx-xx. DOI:https://doi.org/10.5281/zenodo.7124220
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