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Journal Abstract Search

174 related items for PubMed ID: 15351048

  • 1. Development and validation of a fully automated method for the chromatographic determination of content uniformity of drug tablets.
    Toro I, Dulsat JF, Fábregas JL, Claramunt J.
    J Pharm Biomed Anal; 2004 Sep 21; 36(1):57-63. PubMed ID: 15351048
    [Abstract] [Full Text] [Related]

  • 2. Development and validation of a reversed-phase liquid chromatographic method for analysis of degradation products of estradiol in Vagifem tablets.
    Nygaard L, Drøhse Kilde H, Andersen SG, Henriksen L, Overby V.
    J Pharm Biomed Anal; 2004 Feb 04; 34(2):265-76. PubMed ID: 15013140
    [Abstract] [Full Text] [Related]

  • 3. Development and validation of a new HPLC analytical method for the determination of alprazolam in tablets.
    Pérez-Lozano P, García-Montoya E, Orriols A, Miñarro M, Ticó JR, Suñé-Negre JM.
    J Pharm Biomed Anal; 2004 Mar 10; 34(5):979-87. PubMed ID: 15019032
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Development and validation of an analytical method for metformin hydrochloride and its related compound (1-cyanoguanidine) in tablet formulations by HPLC-UV.
    Al-Rimawi F.
    Talanta; 2009 Oct 15; 79(5):1368-71. PubMed ID: 19635372
    [Abstract] [Full Text] [Related]

  • 6. Validation of a dissolution method with HPLC analysis for lasofoxifene tartrate low dose tablets.
    Space JS, Opio AM, Nickerson B, Jiang H, Dumont M, Berry M.
    J Pharm Biomed Anal; 2007 Sep 03; 44(5):1064-71. PubMed ID: 17560750
    [Abstract] [Full Text] [Related]

  • 7. Development and validation of RP-HPLC and ultraviolet spectrophotometric methods of analysis for the quantitative estimation of antiretroviral drugs in pharmaceutical dosage forms.
    Sarkar M, Khandavilli S, Panchagnula R.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Jan 18; 830(2):349-54. PubMed ID: 16330261
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Development and validation of a new gas flame ionization detector method for the determination of finasteride in tablets.
    Sağlik S, Tatar Ulu S.
    Anal Biochem; 2006 May 15; 352(2):260-4. PubMed ID: 16527234
    [Abstract] [Full Text] [Related]

  • 10. Development and validation of a HPLC method for the analysis of promethazine hydrochloride in hot-melt extruded dosage forms.
    Thumma S, Zhang SQ, Repka MA.
    Pharmazie; 2008 Aug 15; 63(8):562-7. PubMed ID: 18771002
    [Abstract] [Full Text] [Related]

  • 11. Development and validation of UPLC method for determination of primaquine phosphate and its impurities.
    Dongre VG, Karmuse PP, Rao PP, Kumar A.
    J Pharm Biomed Anal; 2008 Jan 22; 46(2):236-42. PubMed ID: 18029132
    [Abstract] [Full Text] [Related]

  • 12. Application of stability-indicating HPTLC method for quantitative determination of metadoxine in pharmaceutical dosage form.
    Kaul N, Agrawal H, Patil B, Kakad A, Dhaneshwar SR.
    Farmaco; 2005 Apr 22; 60(4):351-60. PubMed ID: 15848212
    [Abstract] [Full Text] [Related]

  • 13. Automated 96-well solid phase extraction and hydrophilic interaction liquid chromatography-tandem mass spectrometric method for the analysis of cetirizine (ZYRTEC) in human plasma--with emphasis on method ruggedness.
    Song Q, Junga H, Tang Y, Li AC, Addison T, McCort-Tipton M, Beato B, Naidong W.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Jan 05; 814(1):105-14. PubMed ID: 15607714
    [Abstract] [Full Text] [Related]

  • 14. Gradient HPLC analysis of raloxifene hydrochloride and its application to drug quality control.
    Basavaiah K, Anil Kumar UR, Tharpa K.
    Acta Pharm; 2008 Sep 05; 58(3):347-56. PubMed ID: 19103571
    [Abstract] [Full Text] [Related]

  • 15. Automated determination of flutamide by a validated flow-injection method: application to dissolution studies of pharmaceutical tablets.
    Tzanavaras PD, Themelis DG.
    J Pharm Biomed Anal; 2007 Apr 11; 43(5):1820-4. PubMed ID: 17197148
    [Abstract] [Full Text] [Related]

  • 16. Automated sample preparation of Roxifiban tablets: transfer of a manual method to an automated workstation.
    Shamrock WF, Reilly K, Lloyd DK.
    J Pharm Biomed Anal; 2000 Jan 11; 21(6):1225-32. PubMed ID: 10708406
    [Abstract] [Full Text] [Related]

  • 17. Simultaneous determination of pioglitazone and glimepiride in bulk drug and pharmaceutical dosage form by RP-HPLC method.
    A K, G S, C MR, Bhat K, A R, P M, M S, K K, N U.
    Pak J Pharm Sci; 2008 Oct 11; 21(4):421-5. PubMed ID: 18930865
    [Abstract] [Full Text] [Related]

  • 18. Validation of direct assay of an aqueous formulation of a drug compound AZY by chiral supercritical fluid chromatography (SFC).
    Mukherjee PS.
    J Pharm Biomed Anal; 2007 Jan 17; 43(2):464-70. PubMed ID: 16930907
    [Abstract] [Full Text] [Related]

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