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Journal Abstract Search

204 related items for PubMed ID: 15019038

  • 1. 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
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  • 2. 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
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  • 3. Separation and characterization of synthetic impurities of triclabendazole by reversed-phase high-performance liquid chromatography/electrospray ionization mass spectrometry.
    Zhou H, Tai Y, Sun C, Pan Y.
    J Pharm Biomed Anal; 2005 Feb 07; 37(1):97-107. PubMed ID: 15664748
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  • 4. 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
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  • 7. Stability-indicating high performance liquid chromatographic method for determination of norfloxacin in bulk form and tablets.
    al-Deeb OA, Abdel-Moety EM, Abounassif MA, Alzaben SR.
    Boll Chim Farm; 1995 Oct 13; 134(9):497-502. PubMed ID: 8527102
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  • 10. A high performance liquid chromatographic procedure for the simultaneous determination of norfloxacin and furprofen in rat plasma.
    Carlucci G, Mazzeo P, Palumbo G.
    Biomed Chromatogr; 1993 Oct 13; 7(3):126-8. PubMed ID: 8318826
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  • 11. Determination and in-process control of zolpidem synthesis by high-performance liquid chromatography.
    Laviana L, Mangas C, Fernández-Marí F, Bayod M, Blanco D.
    J Pharm Biomed Anal; 2004 Nov 19; 36(4):925-8. PubMed ID: 15533692
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  • 12. High performance liquid chromatographic and thin layer densitometric methods for the determination of risperidone in the presence of its degradation products in bulk powder and in tablets.
    El-Sherif ZA, El-Zeany B, El-Houssini OM.
    J Pharm Biomed Anal; 2005 Jan 04; 36(5):975-81. PubMed ID: 15620522
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  • 13. 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
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  • 14. Development and validation of a reversed-phase liquid chromatographic method for analysis of demeclocycline and related impurities.
    Kahsay G, Maxa J, Van Schepdael A, Hoogmartens J, Adams E.
    J Sep Sci; 2012 Jun 19; 35(10-11):1310-8. PubMed ID: 22733511
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  • 15. 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
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  • 18. Development of a method for the determination of vardenafil in human plasma by high performance liquid chromatography with UV detection.
    Carlucci G, Palumbo P, Iuliani P, Palumbo G.
    Biomed Chromatogr; 2009 Jul 13; 23(7):759-63. PubMed ID: 19296519
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  • 20. Use of the zirconia-based stationary phase for separation of ibuprofen and its impurities.
    Kucera R, Sochor J, Klimes J, Dohnal J.
    J Pharm Biomed Anal; 2005 Jul 15; 38(4):609-18. PubMed ID: 15967288
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