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Development and validation of stability indicating HPLC method for Clotrimazole lozenges formulation
Objective: A simple, sensitive, precise and accurate stability-indicating HPLC method has been developed and validated for determination of Clotrimazole (CLOT) in its lozenges dosage form. Methods:Expand
Simultaneous Estimation of Ascorbic Acid and Calcium Pantothenate in Multivitamin and Multimineral Tablets by Reverse-Phase HPLC
The present study describes A RP-HPLC method for simultaneous estimation of Ascorbic acid (AA) & Calcium pantothenate (CP) in a pharmaceutical Multivitamin & Multimineral unit dosage form. TheExpand
Estimation of Stavudine, Lamivudine and Nevirapine by Chemometric UV Spectroscopic Method
A chemometric UV- spectrophotometric method of analysis was successfully developed for the simultaneous determination of stavudine, lamivudine and nevirapine in pharmaceutical formulation. TheExpand
Simultaneous Estimation of Apremilast and Betamethasone Dipropionate in Microsponge-Based Topical Formulation using a Stability Indicating RP-HPLC Method: A Quality-by-Design Approach.
TLDR
A stability-indicating reverse phase high-performance liquid chromatography method was developed and validated for simultaneous quantification of apremilast and betamethasone dipropionate in bulk as well as drug loaded microsponges and can be effectively used to quantify APL and BD. Expand
Analytical Method Development and Validation for HPLC-ECD Determination of Moxifloxacin in Marketed Formulations
An HPLC-ECD analytical method with high reproducibility and wide linearity range has been developed and validated. Moxifloxacin was separated and identified using this method with a simple mobileExpand
Scenario of Generic Drug Regulations for ASEAN Countries
South East Asia is a growing pharmaceutical market. The regulatory environment has similar characteristics but drug registration requirements and processes differ among the countries. An AssociationExpand
Stability Indicating Validated UPLC Method for Determination of Nebivolol HCl in Bulk and Pharmaceutical Dosage Form
A simple, rapid, precise and accurate stability indicating ultra-performance liquid chromatography method was developed and validated for the quantitative determination of Nebivolol HCl in bulk drugExpand
Drug product registration and marketing authorization procedures in EU-A perspective
ABSTRACT There are 27 European Union (EU) member states, 3 European Economic Area (EEA) and European Free Trade Association (EFTA) states. For a company willing to market the medicinal product in toExpand
Estimation of Aripiprazole in Bulk Drug and Formulation by UV-Derivative Spectroscopy
Aripiprazole is an atypical neuroleptic drug used to manage conditions like schizophrenia and bipolar disorder. The aim of current work is to compare UV spectrophotometric and derivative techniquesExpand
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