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Journal Abstract Search


438 related items for PubMed ID: 15899567

  • 21. Development and validation of a stability-indicating RP-LC method for famciclovir.
    Raman NV, Harikrishna KA, Prasad AV, Ratnakar Reddy K, Ramakrishna K.
    J Pharm Biomed Anal; 2009 Dec 05; 50(5):797-802. PubMed ID: 19632799
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  • 22. Stability indicating reversed-phase liquid chromatographic determination of metronidazole benzoate and diloxanide furoate as bulk drug and in suspension dosage form.
    Mishal A, Sober D.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):819-23. PubMed ID: 16055294
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  • 23. RP-HPLC method for simultaneous estimation of bisoprolol fumarate and hydrochlorothiazide in tablet formulation.
    Joshi SJ, Karbhari PA, Bhoir SI, Bindu KS, Das C.
    J Pharm Biomed Anal; 2010 Jul 08; 52(3):362-71. PubMed ID: 19926421
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  • 24. A validated reversed phase HPLC method for the determination of process-related impurities in almotriptan malate API.
    Kumar AP, Ganesh VR, Rao DV, Anil C, Rao BV, Hariharakrishnan VS, Suneetha A, Sundar BS.
    J Pharm Biomed Anal; 2008 Mar 13; 46(4):792-8. PubMed ID: 18191357
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  • 25. Stress degradation study on sulfadimethoxine and development of a validated stability-indicating HPLC assay.
    Louati K, Mistiri F, Kallel M, Safta F.
    Ann Pharm Fr; 2011 Mar 13; 69(2):91-9. PubMed ID: 21440101
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  • 26. Isolation and characterization of degradation products of citalopram and process-related impurities using RP-HPLC.
    Rao RN, Raju AN, Narsimha R.
    J Sep Sci; 2008 Jun 13; 31(10):1729-38. PubMed ID: 18481321
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  • 27. Quantitative determination of insulin entrapment efficiency in triblock copolymeric nanoparticles by high-performance liquid chromatography.
    Xu X, Fu Y, Hu H, Duan Y, Zhang Z.
    J Pharm Biomed Anal; 2006 Apr 11; 41(1):266-73. PubMed ID: 16303273
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  • 28. Fesoterodine stress degradation behavior by liquid chromatography coupled to ultraviolet detection and electrospray ionization mass spectrometry.
    Sangoi MS, Todeschini V, Steppe M.
    Talanta; 2011 May 30; 84(4):1068-79. PubMed ID: 21530781
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  • 29. Development and validation of a liquid chromatographic method for the analysis of capreomycin sulfate and its related substances.
    Mallampati S, Huang S, Ashenafi D, Van Hemelrijck E, Hoogmartens J, Adams E.
    J Chromatogr A; 2009 Mar 20; 1216(12):2449-55. PubMed ID: 19185869
    [Abstract] [Full Text] [Related]

  • 30. Development and validation of a gradient HPLC method for the determination of clindamycin and related compounds in a novel tablet formulation.
    Platzer DJ, White BA.
    J Pharm Biomed Anal; 2006 Apr 11; 41(1):84-8. PubMed ID: 16298506
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  • 31. Determination of nelfinavir mesylate as bulk drug and in pharmaceutical dosage form by stability indicating HPLC.
    Jing Q, Shen Y, Tang Y, Ren F, Yu X, Hou Z.
    J Pharm Biomed Anal; 2006 Jun 07; 41(3):1065-9. PubMed ID: 16545536
    [Abstract] [Full Text] [Related]

  • 32. Development of a validated RP-LC/ESI-MS-MS method for separation, identification and determination of related substances of tamsulosin in bulk drugs and formulations.
    Nageswara Rao R, Kumar Talluri MV, Narasa Raju A, Shinde DD, Ramanjaneyulu GS.
    J Pharm Biomed Anal; 2008 Jan 07; 46(1):94-103. PubMed ID: 17951020
    [Abstract] [Full Text] [Related]

  • 33. A validated stability indicating LC method for oxcarbazepine.
    Pathare DB, Jadhav AS, Shingare MS.
    J Pharm Biomed Anal; 2007 Apr 11; 43(5):1825-30. PubMed ID: 17223301
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  • 34. A stability-indicating HPLC assay with diode array detection for the determination of a benzylpenicillin prodrug in aqueous solutions.
    Jain R, Wu Z, Tucker IG.
    J Pharm Biomed Anal; 2009 Dec 05; 50(5):841-6. PubMed ID: 19640667
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  • 35. A stability-indicating high performance liquid chromatographic assay for the determination of orlistat in capsules.
    Mohammadi A, Haririan I, Rezanour N, Ghiasi L, Walker RB.
    J Chromatogr A; 2006 May 26; 1116(1-2):153-7. PubMed ID: 16603170
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  • 36. Determination of omeprazole in human plasma by liquid chromatography-electrospray quadrupole linear ion trap mass spectrometry.
    Wang J, Wang Y, Fawcett JP, Wang Y, Gu J.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):631-5. PubMed ID: 15941642
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  • 37. Determination of zolmitriptan in human plasma by liquid chromatography-tandem mass spectrometry method: application to a pharmacokinetic study.
    Chen X, Liu D, Luan Y, Jin F, Zhong D.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Feb 17; 832(1):30-5. PubMed ID: 16413836
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  • 38. Development of a rapid HPLC method for determination of famotidine in human plasma using a monolithic column.
    Zarghi A, Shafaati A, Foroutan SM, Khoddam A.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):677-80. PubMed ID: 15894447
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  • 39. Development and validation of a reversed-phase HPLC method for the determination of ezetimibe in pharmaceutical dosage forms.
    Sistla R, Tata VS, Kashyap YV, Chandrasekar D, Diwan PV.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):517-22. PubMed ID: 15936912
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  • 40. A novel and rapid validated stability-indicating UPLC method of related substances for dorzolamide hydrochloride and timolol maleate in ophthalmic dosage form.
    Sharma N, Rao SS, Reddy AM.
    J Chromatogr Sci; 2012 Oct 15; 50(9):745-55. PubMed ID: 22562819
    [Abstract] [Full Text] [Related]


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