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Journal Abstract Search

352 related items for PubMed ID: 16792063

  • 1. Determination of gatifloxacin in bulk and tablet preparations by high-performance liquid chromatography.
    Salgado HR, Lopes CC.
    J AOAC Int; 2006; 89(3):642-5. PubMed ID: 16792063
    [Abstract] [Full Text] [Related]

  • 2. Determination of lomefloxacin in tablet preparations by liquid chromatography.
    Tozo GC, Salgado HR.
    J AOAC Int; 2006; 89(5):1305-8. PubMed ID: 17042180
    [Abstract] [Full Text] [Related]

  • 3. Simultaneous determination of gatifloxacin and ambroxol hydrochloride from tablet dosage form using reversed-phase high performance liquid chromatography.
    Shahed M, Nanda R, Dehghan MH, Nasreen H, Feroz S.
    Se Pu; 2008 May; 26(3):358-61. PubMed ID: 18724676
    [Abstract] [Full Text] [Related]

  • 4. 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 23; 40(1):179-84. PubMed ID: 16095864
    [Abstract] [Full Text] [Related]

  • 5. LC determination of enrofloxacin.
    e Souza MJ, Bittencourt CF, Morsch LM.
    J Pharm Biomed Anal; 2002 Jun 15; 28(6):1195-9. PubMed ID: 12049983
    [Abstract] [Full Text] [Related]

  • 6. Development of a new high-performance liquid chromatographic method for the determination of ceftazidime.
    Moreno Ade H, Salgado HR.
    J AOAC Int; 2008 Jun 15; 91(4):739-43. PubMed ID: 18727531
    [Abstract] [Full Text] [Related]

  • 7. Simultaneous determination of cefixime trihydrate and dicloxacillin sodium in pharmaceutical dosage form by reversed-phase high-performance liquid chromatography.
    Dhoka MV, Sandage SJ, Dumbre SC.
    J AOAC Int; 2010 Jun 15; 93(2):531-5. PubMed ID: 20480900
    [Abstract] [Full Text] [Related]

  • 8. Determination of linezolid in pharmaceutical dosage forms by liquid chromatography and ultraviolet spectroscopy.
    Patel SA, Patel PU, Patel NJ, Patel MM, Bangoriya UV.
    J AOAC Int; 2007 Jun 15; 90(5):1272-7. PubMed ID: 17955972
    [Abstract] [Full Text] [Related]

  • 9. Determination of tadalafil in pure powder and tablet dosage form by high-performance liquid chromatography.
    Barot TG, Patel PK.
    J AOAC Int; 2010 Jun 15; 93(2):516-22. PubMed ID: 20480898
    [Abstract] [Full Text] [Related]

  • 10. Development of a simple and sensitive high-performance liquid chromatography method for determination of glucosamine in pharmaceutical formulations.
    Nemati M, Valizadeh H, Ansarin M, Ghaderi F.
    J AOAC Int; 2007 Jun 15; 90(2):354-7. PubMed ID: 17474504
    [Abstract] [Full Text] [Related]

  • 11. Development and validation of an ion-pairing RP-HPLC method for the estimation of gatifloxacin in bulk and formulations.
    Venugopal K, Snehalatha M, Bende G, Saha R.
    J Chromatogr Sci; 2007 Apr 15; 45(4):220-5. PubMed ID: 17504572
    [Abstract] [Full Text] [Related]

  • 12. Development and validation of an HPLC method for the determination of gatifloxacin stability in human plasma.
    Al-Dgither S, Alvi SN, Hammami MM.
    J Pharm Biomed Anal; 2006 Apr 11; 41(1):251-5. PubMed ID: 16311002
    [Abstract] [Full Text] [Related]

  • 13. Determination of tianeptine in tablets by high-performance liquid chromatography with fluorescence detection.
    Ulu ST.
    J AOAC Int; 2007 Apr 11; 90(3):720-4. PubMed ID: 17580625
    [Abstract] [Full Text] [Related]

  • 14. Development and validation of a HPLC method for the determination of buprenorphine hydrochloride, naloxone hydrochloride and noroxymorphone in a tablet formulation.
    Mostafavi A, Abedi G, Jamshidi A, Afzali D, Talebi M.
    Talanta; 2009 Feb 15; 77(4):1415-9. PubMed ID: 19084658
    [Abstract] [Full Text] [Related]

  • 15. A stability-indicating high-performance liquid chromatographic method for the determination of methocarbamol in veterinary preparations.
    Rosasco MA, Ceresole R, Forastieri CC, Segall AI.
    J AOAC Int; 2009 Feb 15; 92(5):1602-5. PubMed ID: 19916399
    [Abstract] [Full Text] [Related]

  • 16. Determination of leflunomide in tablets by high performance liquid chromatography.
    Yeniceli D, Dogrukol-Ak D, Tuncel M.
    J Pharm Biomed Anal; 2006 Jan 23; 40(1):197-201. PubMed ID: 16112831
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. 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 Sep 15; 90(5):1242-9. PubMed ID: 17955968
    [Abstract] [Full Text] [Related]

  • 19. Development and validation of an HPLC-UV method for the determination of gatifloxacin in bulk material, pharmaceutical formulations, human plasma and metal complexes.
    Sultana N, Arayne MS, Naz A.
    Pak J Pharm Sci; 2006 Oct 15; 19(4):275-81. PubMed ID: 17105703
    [Abstract] [Full Text] [Related]

  • 20. Development and validation of an UV spectrophotometric method for determination of gatifloxacin in tablets.
    Salgado HR, Oliveira CL.
    Pharmazie; 2005 Apr 15; 60(4):263-4. PubMed ID: 15881604
    [Abstract] [Full Text] [Related]

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