Development and validation of stability-indicating RP-HPLC method for the determination of Levocabastine HCl in bulk drug and in ophthalmic suspensions
A new stability-indicating RP-HPLC assay method was developed and validated for quantitative determination of Levocabastine HCl in bulk drugs and in ophthalmic suspensions in the presence of degradation products generated from forced degradation studies. The system consisted of Thermo Hypersil CPS c...
Main Authors: | Hashem AlAani, Iman Alashkar, François Karabet |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2017-05-01
|
Series: | Arabian Journal of Chemistry |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1878535213004218 |
Similar Items
-
The Early Efficacy of Topical Levocabastine in Patients with Allergic Conjunctivitis
by: Hiroshi Fujishima, et al.
Published: (2006-01-01) -
Practical and Sustainable Synthesis of Optically Pure Levocabastine, a H1 Receptor Antagonist
by: Sung Kwon Kang, et al.
Published: (2017-11-01) -
Simultaneous estimation for Dicyclomine HCl and Simethicone in bulk and oral liquid drop formulation: an RP-HPLC method development and validation
by: Pradeep Kumar Pandey, et al.
Published: (2020-05-01) -
Development and validation of stability-indicating RP-HPLC method for the simultaneous determination of ertugliflozin pidolate and metformin hydrochloride in bulk and tablets
by: K. Sravana Kumari, et al.
Published: (2020-10-01) -
Stability-indicating RP-HPLC method applied to the quantification of anti-histaminic drug ebastine in its oral suspension dosage form
by: Swathi Koduru, et al.
Published: (2023-01-01)