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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

307 related items for PubMed ID: 15533668

  • 1. Development and validation of a liquid chromatographic method for determination of related-substances of mosapride citrate in bulk drugs and pharmaceuticals.
    Nageswara Rao R, Nagaraju D, Alvi SN, Bhirud SB.
    J Pharm Biomed Anal; 2004 Nov 19; 36(4):759-67. PubMed ID: 15533668
    [Abstract] [Full Text] [Related]

  • 2. Enantioselective determination of a gastroprokinetic drug using amylose tris-(3,5-dimethylphenylcarbamate) as a stationary phase by HPLC.
    Nageswara Rao R, Nagaraju D, Narasaraju A.
    J Pharm Biomed Anal; 2006 Feb 13; 40(2):338-44. PubMed ID: 16311003
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Simultaneous separation and determination of coenzyme Q(10) and its process related impurities by NARP-HPLC and atmospheric pressure chemical ionization-mass spectrometry (APCI-MS).
    Nageswara Rao R, Kumar Talluri MV, Shinde DD.
    J Pharm Biomed Anal; 2008 Jun 09; 47(2):230-7. PubMed ID: 18243624
    [Abstract] [Full Text] [Related]

  • 5. A validated RP-HPLC method for the determination of mosapride citrate in bulk drug samples and pharmaceutical formulations.
    Krishnaiah YS, Murthy TK, Sankar DG, Satyanarayana V.
    Pharmazie; 2002 Dec 09; 57(12):814-6. PubMed ID: 12561242
    [Abstract] [Full Text] [Related]

  • 6. Development and validation of a reversed phase liquid chromatographic method for separation and determination of related-substances of modafinil in bulk drugs.
    Nageswara Rao R, Shinde DD, Kumar Talluri MV.
    Talanta; 2007 Sep 30; 73(3):407-14. PubMed ID: 19073048
    [Abstract] [Full Text] [Related]

  • 7. Liquid chromatography-tandem mass spectrometric method for determination of mosapride citrate in equine tissues.
    Aoki Y, Hakamata H, Igarashi Y, Uchida K, Kobayashi H, Hirayama N, Kotani A, Kusu F.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Oct 15; 858(1-2):135-42. PubMed ID: 17851144
    [Abstract] [Full Text] [Related]

  • 8. Separation and determination of synthetic impurities of difloxacin by reversed-phase high-performance liquid chromatography.
    Rao RN, Nagaraju V.
    J Pharm Biomed Anal; 2004 Nov 19; 36(4):729-35. PubMed ID: 15533664
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Development and validation of a liquid chromatographic method for the simultaneous determination of aniracetam and its related substances in the bulk drug and a tablet formulation.
    Papandreou G, Zorpas K, Archontaki H.
    J Pharm Biomed Anal; 2011 Nov 01; 56(3):615-22. PubMed ID: 21742456
    [Abstract] [Full Text] [Related]

  • 11. High-performance liquid chromatographic method for the determination of moclobemide and its two major metabolites in human plasma.
    Rakic A, Miljkovic B, Pokrajac M, Vucicevic K.
    J Pharm Biomed Anal; 2007 Mar 12; 43(4):1416-22. PubMed ID: 17141442
    [Abstract] [Full Text] [Related]

  • 12. Isolation and characterization of process related impurities and degradation products of bicalutamide and development of RP-HPLC method for impurity profile study.
    Nageswara Rao R, Narasa Raju A, Narsimha R.
    J Pharm Biomed Anal; 2008 Feb 13; 46(3):505-19. PubMed ID: 18162355
    [Abstract] [Full Text] [Related]

  • 13. A novel validated LC method for quantitation of lopinavir in bulk drug and pharmaceutical formulation in the presence of its potential impurities and degradation products.
    Seshachalam U, Haribabu B, Chandrasekhar K.
    Biomed Chromatogr; 2007 Jul 13; 21(7):716-23. PubMed ID: 17370253
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Enantiomeric separation of S-zopiclone and its R-enantiomer in bulk drug samples by validated chiral RP-HPLC.
    Sangaraju S, Lakshmi Kanth M, Rao BM, Someswararao N.
    Pharmazie; 2009 Nov 13; 64(11):717-9. PubMed ID: 20099514
    [Abstract] [Full Text] [Related]

  • 18. Separation and determination of synthetic impurities of norfloxacin by reversed-phase high performance liquid chromatography.
    Nageswara Rao R, Nagaraju V.
    J Pharm Biomed Anal; 2004 Mar 10; 34(5):1049-56. PubMed ID: 15019038
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.