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Journal Abstract Search

352 related items for PubMed ID: 17370253

  • 21. Application of a validated stability-indicating densitometric thin-layer chromatographic method to stress degradation studies on moxifloxacin.
    Motwani SK, Khar RK, Ahmad FJ, Chopra S, Kohli K, Talegaonkar S.
    Anal Chim Acta; 2007 Jan 16; 582(1):75-82. PubMed ID: 17386477
    [Abstract] [Full Text] [Related]

  • 22. A stability indicating LC method for rivastigmine hydrogen tartrate.
    Rao BM, Srinivasu MK, Kumar KP, Bhradwaj N, Ravi R, Mohakhud PK, Reddy GO, Kumar PR.
    J Pharm Biomed Anal; 2005 Feb 07; 37(1):57-63. PubMed ID: 15664743
    [Abstract] [Full Text] [Related]

  • 23. Development and validation of HPLC method for the determination of Cyclosporin A and its impurities in Neoral capsules and its generic versions.
    Bonifacio FN, Giocanti M, Reynier JP, Lacarelle B, Nicolay A.
    J Pharm Biomed Anal; 2009 Feb 20; 49(2):540-6. PubMed ID: 19124213
    [Abstract] [Full Text] [Related]

  • 24. Validated stability-indicating HPLC method for the determination of dimethyl-4,4'-dimethoxy-5,6,5',6'-dimethylene dioxybiphenyl-2,2'-dicarboxylate (DDB) and its degradation products.
    Hadad GM.
    J Pharm Biomed Anal; 2008 Aug 05; 47(4-5):695-703. PubMed ID: 18403161
    [Abstract] [Full Text] [Related]

  • 25. Validation of a HPLC method for the quantification and purity determination of SK3530 in drug substance and tablet.
    Oh JG, Jang WJ, Chi SC.
    J Pharm Biomed Anal; 2007 Feb 19; 43(3):1179-84. PubMed ID: 17134866
    [Abstract] [Full Text] [Related]

  • 26. LC and LC-MS study of stress decomposition behaviour of isoniazid and establishment of validated stability-indicating assay method.
    Bhutani H, Singh S, Vir S, Bhutani KK, Kumar R, Chakraborti AK, Jindal KC.
    J Pharm Biomed Anal; 2007 Mar 12; 43(4):1213-20. PubMed ID: 17118610
    [Abstract] [Full Text] [Related]

  • 27. A validated stability indicating ion-pair RP-LC method for zoledronic acid.
    Rao BM, Srinivasu MK, Rani ChP, kumar SS, Kumar PR, Chandrasekhar KB, Veerender M.
    J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):781-90. PubMed ID: 15922532
    [Abstract] [Full Text] [Related]

  • 28. 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 15; 69(2):91-9. PubMed ID: 21440101
    [Abstract] [Full Text] [Related]

  • 29. High performance liquid chromatographic analysis of dehydroepiandrosterone and its pharmaceutical tablet formulation.
    Aboul-Enein HY.
    Biomed Chromatogr; 2004 Jan 15; 18(1):6-9. PubMed ID: 14872542
    [Abstract] [Full Text] [Related]

  • 30. Stability-indicating UPLC method for determination of Valsartan and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms.
    Krishnaiah Ch, Reddy AR, Kumar R, Mukkanti K.
    J Pharm Biomed Anal; 2010 Nov 02; 53(3):483-9. PubMed ID: 20646890
    [Abstract] [Full Text] [Related]

  • 31. Stability indicating validated HPLC method for quantification of levothyroxine with eight degradation peaks in the presence of excipients.
    Shah RB, Bryant A, Collier J, Habib MJ, Khan MA.
    Int J Pharm; 2008 Aug 06; 360(1-2):77-82. PubMed ID: 18524511
    [Abstract] [Full Text] [Related]

  • 32. 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]

  • 33. LC determination of glimepiride and its related impurities.
    Khan MA, Sinha S, Vartak S, Bhartiya A, Kumar S.
    J Pharm Biomed Anal; 2005 Oct 04; 39(5):928-43. PubMed ID: 16040224
    [Abstract] [Full Text] [Related]

  • 34. Quantitation of alfuzosin hydrochloride in pharmaceutical formulations by RP-HPLC.
    Ganesh M, Uppatyay S, Tivari R, Kamalakannan K, Rathinavel G, Gangully S, Sivakumar T.
    Pak J Pharm Sci; 2009 Jul 04; 22(3):263-6. PubMed ID: 19553171
    [Abstract] [Full Text] [Related]

  • 35. 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]

  • 36. Quantitation of buclizine hydrochloride in pharmaceutical formulations and human serum by RP-HPLC.
    Arayne MS, Sultana N, Siddiqui FA.
    Pak J Pharm Sci; 2006 Oct 15; 19(4):326-9. PubMed ID: 17105713
    [Abstract] [Full Text] [Related]

  • 37. Development of a validated liquid chromatographic method for the determination of related substances and assay of tenofovir disoproxil fumarate.
    Ashenafi D, Chintam V, van Veghel D, Dragovic S, Hoogmartens J, Adams E.
    J Sep Sci; 2010 Jun 15; 33(12):1708-16. PubMed ID: 20446297
    [Abstract] [Full Text] [Related]

  • 38. 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 15; 60(4):351-60. PubMed ID: 15848212
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. Determination of duloxetine hydrochloride in the presence of process and degradation impurities by a validated stability-indicating RP-LC method.
    Raman NV, Harikrishna KA, Prasad AV, Reddy KR, Ramakrishna K.
    J Pharm Biomed Anal; 2010 Mar 11; 51(4):994-7. PubMed ID: 20005658
    [Abstract] [Full Text] [Related]

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