These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
318 related articles for article (PubMed ID: 15936912)
21. A stability indicating LC method for zolmitriptan. Rao BM; Srinivasu MK; Sridhar G; Kumar PR; Chandrasekhar KB; Islam A J Pharm Biomed Anal; 2005 Sep; 39(3-4):503-9. PubMed ID: 15899567 [TBL] [Abstract][Full Text] [Related]
22. Quantitation of buclizine hydrochloride in pharmaceutical formulations and human serum by RP-HPLC. Arayne MS; Sultana N; Siddiqui FA Pak J Pharm Sci; 2006 Oct; 19(4):326-9. PubMed ID: 17105713 [TBL] [Abstract][Full Text] [Related]
24. Development and validation of RP-HPLC method for the analysis of metformin. Arayne MS; Sultana N; Zuberi MH Pak J Pharm Sci; 2006 Jul; 19(3):231-5. PubMed ID: 16935831 [TBL] [Abstract][Full Text] [Related]
25. Simultaneous quantification of stavudine, lamivudine and nevirapine by UV spectroscopy, reverse phase HPLC and HPTLC in tablets. Anbazhagan S; Indumathy N; Shanmugapandiyan P; Sridhar SK J Pharm Biomed Anal; 2005 Sep; 39(3-4):801-4. PubMed ID: 15950425 [TBL] [Abstract][Full Text] [Related]
26. Developing and optimizing a validated isocratic reversed-phase high-performance liquid chromatography separation of nimodipine and impurities in tablets using experimental design methodology. Barmpalexis P; Kanaze FI; Georgarakis E J Pharm Biomed Anal; 2009 Jul; 49(5):1192-202. PubMed ID: 19369025 [TBL] [Abstract][Full Text] [Related]
27. Development and validation of RP-HPLC method for cetrimonium bromide and lidocaine determination. Malenovic A; Medenica M; Ivanovic D; Jancic B; Markovic S Farmaco; 2005 Feb; 60(2):157-61. PubMed ID: 15752474 [TBL] [Abstract][Full Text] [Related]
28. Development and validation of a simple reversed-phase high-performance liquid chromatography method for the determination of testosterone in serum of males. Loi V; Vertzoni M; Vryonidou A; Phenekos C J Pharm Biomed Anal; 2006 May; 41(2):527-32. PubMed ID: 16406451 [TBL] [Abstract][Full Text] [Related]
29. Optimization of separation and determination of moxifloxacin and its related substances by RP-HPLC. Djurdjevic P; Ciric A; Djurdjevic A; Stankov MJ J Pharm Biomed Anal; 2009 Sep; 50(2):117-26. PubMed ID: 19464135 [TBL] [Abstract][Full Text] [Related]
30. Concurrent determination of ezetimibe and its phase-I and II metabolites by HPLC with UV detection: quantitative application to various in vitro metabolic stability studies and for qualitative estimation in bile. Basha SJ; Naveed SA; Tiwari NK; Shashikumar D; Muzeeb S; Kumar TR; Kumar NV; Rao NP; Srinivas N; Mullangi R; Srinivas NR J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Jun; 853(1-2):88-96. PubMed ID: 17442643 [TBL] [Abstract][Full Text] [Related]
31. Quantitative determination of gatifloxacin, levofloxacin, lomefloxacin and pefloxacin fluoroquinolonic antibiotics in pharmaceutical preparations by high-performance liquid chromatography. Santoro MI; Kassab NM; Singh AK; Kedor-Hackmam ER J Pharm Biomed Anal; 2006 Jan; 40(1):179-84. PubMed ID: 16095864 [TBL] [Abstract][Full Text] [Related]
32. Stability-indicating reversed-phase liquid chromatographic method for simultaneous determination of simvastatin and ezetimibe from their combination drug products. Chaudhari BG; Patel NM; Shah PB J AOAC Int; 2007; 90(5):1242-9. PubMed ID: 17955968 [TBL] [Abstract][Full Text] [Related]
33. Development and validation of a rapid reversed-phase HPLC method for the determination of insulin from nanoparticulate systems. Sarmento B; Ribeiro A; Veiga F; Ferreira D Biomed Chromatogr; 2006 Sep; 20(9):898-903. PubMed ID: 16389645 [TBL] [Abstract][Full Text] [Related]
34. Stability-indicating reversed-phase liquid chromatographic method for simultaneous determination of atorvastatin and ezetimibe from their combination drug products. Chaudhari BG; Patel NM; Shah PB; Patel LJ; Patel VP J AOAC Int; 2007; 90(6):1539-46. PubMed ID: 18193730 [TBL] [Abstract][Full Text] [Related]
36. Identification, isolation and characterization of process related impurities in ezetimibe. Guntupalli S; Ray UK; Murali N; Gupta PB; Kumar VJ; Satheesh D; Islam A J Pharm Biomed Anal; 2014 Jan; 88():385-90. PubMed ID: 24176742 [TBL] [Abstract][Full Text] [Related]
37. High performance liquid chromatographic determination of 3-methylflavone-8-carboxylic acid, the main active metabolite of flavoxate hydrochloride in human urine. El-Gindy A; Sallam S; Abdel-Salam RA J Pharm Biomed Anal; 2007 May; 44(1):274-8. PubMed ID: 17349765 [TBL] [Abstract][Full Text] [Related]
38. Development and validation of spectrophotometeric method for simultaneous determination of simvastatin and ezetimibe in tablet formulations. Balaji S; Sunitha A Pak J Pharm Sci; 2010 Oct; 23(4):375-8. PubMed ID: 20884449 [TBL] [Abstract][Full Text] [Related]
39. Development and validation of high performance liquid chromatography method for analysis of sibutramine hydrochloride and its impurity. Chandorkar JG; Kotwal VB; Dhande NS; Pachpor MP; Pande VV Pak J Pharm Sci; 2008 Apr; 21(2):121-4. PubMed ID: 18390441 [TBL] [Abstract][Full Text] [Related]
40. Development and validation of a high-performance liquid chromatographic method for the analysis of budesonide. Gupta M; Bhargava HN J Pharm Biomed Anal; 2006 Feb; 40(2):423-8. PubMed ID: 16143482 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]