| A validated stability-indicating LC method for acetazolamide in the presence of degradation products and its process-related impurities P Srinivasu, DV SubbaRao, RVK Vegesna, KS Babu Journal of pharmaceutical and biomedical analysis 52 (1), 142-148, 2010 | 34 | 2010 |
| New RP-HPLC method for the determination of olmesartan medoxomil in tablet dosage form RB Ganduri, RA Lanka, S Pamidi, JR Peddareddigari, M Mohammed Eurasian J Anal Chem 5 (2), 145-51, 2010 | 33 | 2010 |
| Development and validation of a new LC method for analysis of brimonidine tartrate and related compounds A Madhavi, A Naidu, DV Subba Rao, P Srinivasu Chromatographia 69, 1413-1419, 2009 | 21 | 2009 |
| Development and validation of a new analytical method for the determination of related components and assay of ranolazine in bulk drug and pharmaceutical dosage forms by LC A Madhavi, DV Subba Rao, P Srinivasu, A Naidu Chromatographia 70, 333-338, 2009 | 19 | 2009 |
| A stability-indicating UPLC method for the determination of potential impurities and its mass by a new QDa mass detector in daclatasvir drug used to treat hepatitis C infection V Jagadabi, PV Nagendra Kumar, K Mahesh, S Pamidi, LA Ramaprasad, ... Journal of chromatographic science 57 (1), 44-53, 2019 | 18 | 2019 |
| Development and validation of stability indicating HPLC method for combination tablet dosage form of efavirenz, lamivudine and tenofovir in tablet CHV Reddiah, PR Devi, K Mukkanti, P Srinivasu International Journal of Pharmaceutical and Phytopharmacological Research 2 …, 2012 | 13 | 2012 |
| New RP-HPLC method for the determination of darunavir in tablet dosage form RB Ganduri, RA Lanka, S Pamidi, JR Peddareddigari, J Rao Asian J. Pharm. Res 1 (1), 10-14, 2011 | 12 | 2011 |
| NEW RAPID UPLC METHOD FOR THE ESTIMATION OF IMPURITIES IN THE CAPSULE DOSAGE FORM OF SILODOSIN S Kishore Kumar Hotha Lanka A.Rama Prasad , J.V.L.N International Journal of Analytical and Bioanalytical Chemistry 2 (4), 24-251, 2012 | 9* | 2012 |
| Stability indicating HPLC method for impurities estimation of nevirapine in extended release tablet dose CV Reddiah, PR Devi, K Mukkanti, P Srinivasu Pharmacophore 4 (2), 2013 | 8 | 2013 |
| UPLC METHOD FOR THE DETERMINATION OF ESZOPICLONE AND ITS RELATED IMPURITIES S Kishore Kumar Hotha Lanka A.Rama Prasad , J.V.L.N International Journal of Analytical and Bioanalytical Chemistry 2 (4), 241-246, 2012 | 8* | 2012 |
| New RP-HPLC method for the determination of darunavir in tablet dosage form BG Raveendra, LA Ramprasad, P Srinivasu, RP Jayachandra, J Rao Asian Journal of Pharmaceutical Research 1, 10-14, 2011 | 7 | 2011 |
| A validated stability-indicating LC method for fluocinonide in the presence of degradation products, its process-related impurities and identification of degradation products P Srinivasu, DV SubbaRao, RVK Vegesna, KS Babu American Journal of Analytical Chemistry 1 (03), 113, 2010 | 7 | 2010 |
| A stability-indicating HPLC method for the determination of potential impurities in a new fixed dose combination of dolutegravir, lamivudine and tenofovir disoproxil fumarate … V Jagadabi, P Nagendra Kumar, S Pamidi, L Ramaprasad, D Nagaraju Int Res J Pharm 9 (5), 65-74, 2018 | 6 | 2018 |
| A novel stability-indicating RP-UPLC method for the quantification of impurities and a new QDa mass detector coupled with LC–PDA for identification of mass of degradation … V Jagadabi, PVN Kumar, S Pamidi, LA Ramaprasad, D Nagaraju International Research Journal of Pharmacy 9 (7), 192-201, 2018 | 6 | 2018 |
| A new RP-HPLC method development for the simultaneous estimation of emtricitabine, efavirenz and tenofovir in tablet dosage form C Palavan, LA Ramprasad, P Srinivasu, J Sheshagirirao American Journal of PharmaTech Research 3, 547-554, 2013 | 6 | 2013 |
| DEVELOPMENT AND VALIDATION OF A NEW STABILITY INDICATING HPLC METHOD FOR QUANTIFICATION OF PROCESS RELATED AND DEGRADATION IMPURITIES OF BICALUTAMIDE IN TABLET DOSAGE FORMS JR Lanka A. Rama Prasad1 and Srinivasu Pamidi1 International journal of Pharmacy 1 (2), 218-223, 2012 | 5* | 2012 |
| Development of stability indicating assay method for separation and identification of degradation products of daclatasvir dihydrochloride by LC-ESI-QTOF-MS/MS D Swain, AS Yadav, V Akula, S Pamidi, G Samanthula Analytical Chemistry Letters 9 (2), 209-222, 2019 | 3 | 2019 |
| NEW STABILITY INDICATING HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF LAMIVUDINE, TENOFOVIR DF AND NEVIRAPINE IN EXTENDED RELEASE TABLETS S . Vara Prasad and J. Hemalatha Lanka A. Rama INTERNATIONAL JOURNAL OF PHARMACY 3 (1), 136-144, 2013 | 3 | 2013 |
| NEW STABILITY INDICATING RP-LC METHOD FOR SIMULTANEOUS QUANTIFICATION OF RELATED IMPURITIES OF LAMIVUDINE, TENOFOVIR DISOPEOXIL FUMARATE AND NEVIRAPINE IN EXTENDED RELEASE … P Goli.Pavani Lanka A.Rama Prasad*, J.V.L.N.S.Rao International Research Journal of Pharmacy 3 (11), 103-108, 2012 | 2 | 2012 |
| Identification, characterization of degradation component in desoximetasone pharmaceutical dosage forms and its quantification in the presence of process related impurities P Srinivasu, K Sudhakarbabu, J Sreeramulu Journal of liquid chromatography & related technologies 35 (8), 1114-1129, 2012 | 2 | 2012 |
