Author(s):
Monika Puri, Yogesh K. Walia
Email(s):
monikapuri20022008@gmail.com , yogesh.che@cpuh.in
DOI:
10.52711/0975-4377.2026.00018 
Address:
Monika Puri1, Yogesh K. Walia2
1Research Scholar, Career Point University, Hamirpur (H.P.), India.
2Professor, Department of Chemistry, Career Point University, Hamirpur (H.P.), India.
*Corresponding Author
Published In:
Volume - 18,
Issue - 2,
Year - 2026
ABSTRACT:
A liquid chromatography method was developed to estimate Rosuvastatin calcium in bulk and pharmaceutical dosage forms accurately. The developed method demonstrates high accuracy, specificity, and reliability, making it particularly suitable for pharmaceutical research. The chromatographic analysis was performed using a C-18 column (250 x 4.6mm, 5µm) with a mobile phase consisting of Acetonitrile and acidified water (pH 3.0 adjusted with orthophosphoric acid) at a ratio of 55:45 v/v. Detection was achieved at a wavelength of 237nm. The retention time for Rosuvastatin Calcium was observed at approximately 7.0 minutes.
Cite this article:
Monika Puri, Yogesh K. Walia. Analytical Method Development and Validation of Antihypertensive Drug: Rosuvastatin Calcium using Reverse Phase-High Performance Liquid Chromatogrhaphic Method. Research Journal of Pharmaceutical Dosage Forms and Technology. 2026; 18(2):115-0. doi: 10.52711/0975-4377.2026.00018
Cite(Electronic):
Monika Puri, Yogesh K. Walia. Analytical Method Development and Validation of Antihypertensive Drug: Rosuvastatin Calcium using Reverse Phase-High Performance Liquid Chromatogrhaphic Method. Research Journal of Pharmaceutical Dosage Forms and Technology. 2026; 18(2):115-0. doi: 10.52711/0975-4377.2026.00018 Available on: https://www.rjpdft.com/AbstractView.aspx?PID=2026-18-2-4
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