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545 related items for PubMed ID: 23552846

  • 1. Stability-indicating LC-UV method for the determination of eszopiclone and degradation impurities in tablet dosage form.
    Shaikh K, Patil A, Gite S.
    J Chromatogr Sci; 2014 Apr; 52(4):293-7. PubMed ID: 23552846
    [Abstract] [Full Text] [Related]

  • 2. A novel validated ultra-performance liquid chromatography Method for separation of eszopiclone impurities and its degradants in drug products.
    Sharma N, Rao SS, Kumar ND, Reddy AM.
    J AOAC Int; 2013 Apr; 96(5):981-6. PubMed ID: 24282935
    [Abstract] [Full Text] [Related]

  • 3. A validated stability-indicating liquid chromatographic method for the determination of retapamulin in topical dosage form.
    Nalwade S, Reddy VR.
    J Chromatogr Sci; 2014 Mar; 52(3):238-45. PubMed ID: 23510782
    [Abstract] [Full Text] [Related]

  • 4. Stability-indicating RP-HPLC method for the quantitative analysis of perindopril erbumine in tablet dosage form.
    Dugga HH, Peraman R, Nayakanti D.
    J Chromatogr Sci; 2014 Apr; 52(4):315-20. PubMed ID: 23690066
    [Abstract] [Full Text] [Related]

  • 5. Development and validation of a stability-indicating RP-HPLC assay method and stress degradation studies on dapiprazole.
    Ramesh T, Rao PN.
    J Chromatogr Sci; 2013 Oct; 51(9):856-60. PubMed ID: 23169931
    [Abstract] [Full Text] [Related]

  • 6. UPLC and LC-MS studies on degradation behavior of irinotecan hydrochloride and development of a validated stability-indicating ultra-performance liquid chromatographic method for determination of irinotecan hydrochloride and its impurities in pharmaceutical dosage forms.
    Kumar N, Sangeetha D, Reddy SP.
    J Chromatogr Sci; 2012 Oct; 50(9):810-9. PubMed ID: 22661461
    [Abstract] [Full Text] [Related]

  • 7. A novel reverse phase stability indicating RP-UPLC method for the quantitative determination of fifteen related substances in Ranolazine drug substance and drug product.
    Malati V, Reddy AR, Mukkanti K, Suryanarayana MV.
    Talanta; 2012 Aug 15; 97():563-73. PubMed ID: 22841123
    [Abstract] [Full Text] [Related]

  • 8. Development of validated stability indicating assay method for simultaneous estimation of metformin hydrochloride and vildagliptin by RP-HPLC.
    Satheeshkumar N, Pradeepkumar M, Shanthikumar S, Rao VJ.
    Drug Res (Stuttg); 2014 Mar 15; 64(3):124-9. PubMed ID: 24081820
    [Abstract] [Full Text] [Related]

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

  • 10. 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 08; 50(9):745-55. PubMed ID: 22562819
    [Abstract] [Full Text] [Related]

  • 11. A validated stability indicating ultra performance liquid chromatographic method for determination of impurities in Esomeprazole magnesium gastro resistant tablets.
    Nalwade SU, Reddy VR, Rao DD, Morisetti NK.
    J Pharm Biomed Anal; 2012 Jan 05; 57():109-14. PubMed ID: 21920688
    [Abstract] [Full Text] [Related]

  • 12. Development and validation of a stability-indicating RP-HPLC method for the simultaneous estimation of process related impurities and degradation products of rasagiline mesylate in pharmaceutical formulation.
    Reddy PS, Sudhakar Babu K, Kumar N.
    J Chromatogr Sci; 2013 Mar 05; 51(3):242-9. PubMed ID: 22988002
    [Abstract] [Full Text] [Related]

  • 13. Simultaneous Determination of Impurities of Atazanavir and Ritonavir in Tablet Dosage Form by Using Reversed-Phase Ultra Performance Liquid Chromatographic Method.
    Mantripragada MKVVN, Rao SV, Nutulapati VVS, Mantena BPV.
    J Chromatogr Sci; 2018 Mar 01; 56(3):270-284. PubMed ID: 29300835
    [Abstract] [Full Text] [Related]

  • 14. Development and validation of a stability-indicating RP-HPLC method for the determination of febuxostat (a xanthine oxidase inhibitor).
    Mukthinuthalapati MA, Bandaru SP, Bukkapatnam V, Mohapatro C.
    J Chromatogr Sci; 2013 Mar 01; 51(10):931-8. PubMed ID: 23204011
    [Abstract] [Full Text] [Related]

  • 15. Stability-indicating RP-HPLC method for the simultaneous determination of escitalopram oxalate and clonazepam.
    Kakde RB, Satone DD, Gadapayale KK, Kakde MG.
    J Chromatogr Sci; 2013 Jul 01; 51(6):490-5. PubMed ID: 23135233
    [Abstract] [Full Text] [Related]

  • 16. Quantification of halobetasol propionate and its impurities present in topical dosage forms by stability-indicating LC method.
    Nalwade S, Reddy VR, Kulkarni D, Todamal S.
    J Chromatogr Sci; 2015 Jan 01; 53(1):127-34. PubMed ID: 24784115
    [Abstract] [Full Text] [Related]

  • 17. Development and validation of a novel stability-indicating HPLC method for the quantitative determination of eleven related substances in ezetimibe drug substance and drug product.
    Luo Z, Deng Z, Liu Y, Wang G, Yang W, Hou C, Tang M, Yang R, Zhou H.
    Talanta; 2015 Jul 01; 139():67-74. PubMed ID: 25882410
    [Abstract] [Full Text] [Related]

  • 18. A validated stability-indicating RP-HPLC method for levofloxacin in the presence of degradation products, its process related impurities and identification of oxidative degradant.
    Lalitha Devi M, Chandrasekhar KB.
    J Pharm Biomed Anal; 2009 Dec 05; 50(5):710-7. PubMed ID: 19632800
    [Abstract] [Full Text] [Related]

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