Open Access Research Article

To Study the Quality Control Parameters for Uncoated Paracetamol & Nimesulide Tablet in Pharmaceutical Industry

Viralbhai A Prajapati1, Mona A Gupta1, CN Patel, Pankaj H Prajapati2, Hitesh D Karen2, Laxman M Prajapati2 and Dhrubo Jyoti Sen3*

1K. B. Institute of Pharmaceutical Education & Research, Kadi Campus, Gh-6, Sector-23, India

2Shri Sarvajanik Pharmacy College, Gujarat Technological University, India

3School of Pharmacy, Techno India University, India

Corresponding Author

Received Date: July 22, 2021;  Published Date: August 26, 2021

Abstract

A pharmaceutical uncoated tablet must satisfy certain standards to claim it to be a quality drug. The quality of any drug in dosage form is its safety, potency, stability, patient acceptability and compliance. The quality of tablet needs to be designed from the product development stage. Quality control test for uncoated tablet is strongly related to final product quality because checks performed during production in order to monitor and if necessary, to adjust the process to ensure that the product conform to its specification are the key for the good or excellence quality of a tablet. The main purpose of quality control test for uncoated tablet is to produce a perfect finished product quality control (FPQC) test for tablet are performed with specific quality control test or parameters within acceptance limit or not. The aim of this to study in process quality control test carried for uncoated Paracetamol & Nimesulide.

Keywords: Quality control; quality control test or parameters for uncoated tablets (Paracetamol & Nimesulide); batch details; Analytical data for compressed tablet; Analytical data for finished stage; specification

Citation
Signup for Newsletter
Scroll to Top