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Vundavilli Jagadeesh Kumar

Observed names: J. K. Vundavilli, Jagadeesh Kumar Vundavilli, V. Jagadeesh Kumar, VUNDAVILLI JAGADEESH KUMAR
Observed institution: Aurobindo Pharma (India)
ORCID: 0000-0003-3798-2506
Observed ORCID: 0000-0003-3798-2506
OpenAlex ID: A5090970989
Identification, isolation and characterization of process related impurities in ezetimibe
2013 · Srikanth Guntupalli, Uttam Kumar Ray, et al. · Journal of Pharmaceutical and Biomedical Analysis · 22
Stability indicating ion chromatography method for the simultaneous determination of ibandronate sodium drug substance and its impurities
2010 · M. Narendra Kumar, K.S.R. Pavan Kumar, et al. · Journal of Pharmaceutical and Biomedical Analysis · 12
Development and validation of a simple and rapid ICP-OES method for quantification of elemental impurities in voriconazole drug substance
2021 · Kishore V. Merusomayajula, Siva Rao Tirukkovalluri, et al. · Future Journal of Pharmaceutical Sciences · 11
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Validation of a sensitive ion chromatography method for determination of monoethylsulfate in Indinavir sulfate drug substance
2009 · S. John Prasanna, Hemant Kumar Sharma, et al. · Journal of Pharmaceutical and Biomedical Analysis · 10
Identification and Characterization of New Degradation Products of Cefepime Dihydrochloride Monohydrate Drug Substance during Stress Stability Studies
2010 · Vundavilli Jagadeesh Kumar, P. Badarinadh Gupta, et al. · Analytical Sciences · 9
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Identification, isolation and characterization of a new degradation product in sultamicillin drug substance
2010 · Vundavilli Jagadeesh Kumar, P. Badarinadh Gupta, et al. · Journal of Pharmaceutical and Biomedical Analysis · 5
Quantification of potential genotoxic impurity in Divalproex sodium drug substance by GC-MS method.
2016 · K. V. S. N. Raju, P. Madhava Reddy, et al. · Der pharmacia lettre · 3
Validation of stability-indicating reverse phase HPLC method for the determination of related substances in dabigatran etexilatemesylate drug substance
2015 · N. Sreenivas, K. Raghu Babu, et al. · Der pharmacia lettre · 3
Development and validation of UPLC methods for the determination of 4-Nitro phthalimide, 5-Bromo phthalide and 5- Amino phthalide, 4-Amino phthalimide contents in Citalopram hydrobromide drug substance
2011 · Karunesh Kumar, T. Ch, et al. · Der pharmacia lettre · 3
Identification and characterization of new impurity in CefotaximeSodium drug substance
2010 · Vundavilli Jagadeesh Kumar, Peruri Badarinadh Gupta, et al. · Der pharma chemica · 3
Method Development and Validation for the Determination of Belzutifan in Biological Samples by Liquid Chromatography and Tandem Mass Spectrometry
2025 · Vasudeva Rao Bobba, Mogili Padma, et al. · Separation Science Plus · 2
Simple and reliable gas chromatography method for the trace level determination of oxalyl chloride content in zolpidem tartrate
2015 · N. Siva Krishna, K. V. S. N. Raju, et al. · Der pharmacia lettre · 2
Development and Validation of an Lc-ms/ms Method for the Quantification of Repotrectinib in Human Plasma
2026 · VASUDEVA RAO BOBBA, MOGILI PADMA, et al. · International Journal of Applied Pharmaceutics · 1
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Quantification of Structurally Alert Mutagenic Impurities in Meropenem Trihydrate Drug Substance by Liquid Chromatography with High Resolution Mass Spectrometer (LC-HRMS)
2024 · Anwar Sulaiman, K. Ramakrishna Reddy, et al. · American Journal of Analytical Chemistry · 1
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Simultaneous and Trace Level Determination of Six Potential Impurities by UPLC-ESI-MS/MS in Antiarrhythmic Drug: Dronedarone Hydrochloride
2020 · K. Durga Raja, V. Saradhi Venkata Ramana, et al. · Asian Journal of Chemistry · 1
Validation of Stability-Indicating Reverse Phase HPLC Method for the Determination of Related Substances in Dapagliflozin Drug Substance
2018 · Goutam Sen, K. Raghu Babu, et al. · American Journal of PharmTech Research · 1
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Identification, Isolation, and Characterization of a New Degradation Impurity in Nafcillin Sodium
2015 · Jagadeesh Kumar Vundavilli · Scientia Pharmaceutica · 1
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Identification, isolation and characterization of a new impurity in cefoxitindrug substance resulting from stress stability studies
2010 · Vundavilli Jagadeesh Kumar, P. Badarinadh Gupta, et al. · Analytical Methods · 1
Determination and validation of Monomethylamine content by Ion Chromatography method in pharmaceutical drug substances
2010 · Karunesh Kumar, Vundavilli Jagadeesh Kumar, et al. · Der pharma chemica · 1
Identification and Characterization of New Impurity in Phenoxybenzamine Hydrochloride Drug Substance
2024 · A. K. Guduri, K. B. Bonige, et al. · Russian Journal of General Chemistry
Isolation and structural elucidation of novel degradant during degradation study of Azilsartan kamedoxomil
2024 · Anil Kumar Guduri, Vundavilli Jagadeesh Kumar, et al. · Journal of Pharmaceutical and Biomedical Analysis Open
Low Level Quantification of Potential Genotoxic Impurities In Telmisartan Drug Substance by HPLC
2021 · K. Srivalli, N. Annapurna, et al. · American Journal of PharmTech Research
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Development and Validation of UPLC-ESI-MS/MS Technique for the Determination of 2-Isopropyl-4-(chloromethyl)thiazole in Ritonavir
2020 · K. Durga Raja, V. Saradhi Venkata Ramana, et al. · Asian Journal of Chemistry
Low Level Quantification of Potential Genotoxic Impurity In Ertapenem Monosodium Drug Substance by HPLC
2018 · Vinay Kumar Patcha, Susheela Bhai Gajbhiye, et al. · American Journal of PharmTech Research
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Low Level Quantification of Potential Genotoxic Impurity in Omeprazole Drug Substance by UPLC
2017 · Vinay Kumar Patcha, Susheela Bhai Gajbhiye, et al. · Der pharma chemica
Works count: 27
Citation count: 92
H-index: 5
I10-index: 4
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