Stability-indicating method for the determination of assay and quantification of impurities in amlodipine–atorvastatin combination dosage form by RP-HPLC-Reference-Cited by-同舟云学术

Stability-indicating method for the determination of assay and quantification of impurities in amlodipine–atorvastatin combination dosage form by RP-HPLC

Published:2017-07-03 Issue:11 Volume:40 Page:576-598
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Sangeetha D.¹,Vadlamudi Manoj Kumar¹²^ORCID

Affiliation:

1. School of Advanced Sciences, VIT University, Vellore, Tamil Nadu, India

2. Analytical Research and Development, Ashland (India) Private Limited, Hyderabad, Telangana, India

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826076.2017.1334215

Reference31 articles.

1. Stability indicating RP-HPLC estimation of atorvastatin calcium and amlodipine besylate in pharmaceutical formulations

2. An HPLC method for the determination of atorvastatin and its impurities in bulk drug and tablets

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