Author(s):
S. Ashutosh Kumar, Manidipa Debnath, J.V.L.N. Seshagiri Rao, D. Gowri Sankar
Email(s):
ashu.mpharm2007@gmail.com
DOI:
Not Available
Address:
S. Ashutosh Kumar1*, Manidipa Debnath2, Dr. J.V.L.N. Seshagiri Rao3, Dr. D. Gowri Sankar4
1Department of Pharmaceutical Analysis and Quality Assurance, AKRG College of Pharmacy, Nallajerla,
West Godavari, 534112, A.P, India
2Department of Pharmaceutics, AKRG College of Pharmacy, Nallajerla, West Godavari, 534112, A.P, India
3Prof. Pharmaceutical Analysis, Yalamarty College of Pharmacy, Tarluwada Visakhapatnam, 530052, A.P, India
4Department of Pharmaceutical Analysis and Quality Assurance, College of Pharmaceutical Sciences,
Andhra University, Visakhapatnam, 530003, A.P
*Corresponding Author
Published In:
Volume - 7,
Issue - 5,
Year - 2014
Cite this article:
S. Ashutosh Kumar, Manidipa Debnath, J.V.L.N. Seshagiri Rao, D. Gowri Sankar. Stability indicating Method Development and Validation for simultaneous estimation of Hydrochlorothiazide, Amlodipine and Olmesartan in tablet dosage form by using RP-HPLC. Asian J. Research Chem. 7(5): May 2014; Page 538-548.