An International, Peer-Reviewed, Open Access Multidisciplinary Pharmacy Journal

Development and validation of stability indicating the RP-HPLC method for the estimation of related compounds of guaifenesin in pharmaceutical dosage forms

Submitted by webadmin on Sat, 10/22/2016 - 11:18
Pharmaceutical Methods,2011,2,4,229-234.
DOI:10.4103/2229-4708.93391
Published:December 2011
Type:Symposium - HPLC

Development and validation of stability indicating the RP-HPLC method for the estimation of related compounds of guaifenesin in pharmaceutical dosage forms

Sunil Pingili Reddy1,2, K. Sudhakar Babu2, Navneet Kumar1, Y. V. V. Sasi Sekhar1

1Dr. Reddy’s Laboratories Ltd., Analytical R and D, IPDO, Bachupally, Hyderabad,

2Department of Chemistry, S. K. University, Anantapur, Andhra Pradesh, India.

Keywords:Degradation, Development, guaifenesin, HPLC, impurity, stabilityindicating, validation

View:

  • PDF (487.44 KB)

[Print -2229-4708, Online - 2229-4716]

Copyright © 2019 Phcog.Net. All rights reserved.

Published in cooperation with EManuscript