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Journal Abstract Search

1601 related items for PubMed ID: 22661461

  • 21. Novel Validated Stability-Indicating UPLC Method for the Estimation of Naproxen and its Impurities in Bulk Drugs and Pharmaceutical Dosage Form.
    Venkatarao P, Nagendra Kumar M, Ravi Kumar M.
    Sci Pharm; 2012; 80(4):965-76. PubMed ID: 23264943
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  • 22. A validated stability-indicating UPLC method for the determination of impurities in Maraviroc.
    Chilukuri M, Hussainreddy K, Narayanareddy P, Venkataramana M.
    J Chromatogr Sci; 2014 Aug; 52(7):609-16. PubMed ID: 23825352
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  • 23. Rapid quantitative determination of related substances and degradants in milnacipran.
    Pydimarry SP, Cholleti VK, Venagala RR.
    J Chromatogr Sci; 2014 Jan; 52(1):42-51. PubMed ID: 23258392
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  • 24. A stability-indicating HPLC method for the determination of bazedoxifene acetate and its related substances in active pharmaceutical ingredient.
    Visweswara Rao K, Reddy KP, Kumari KS, Srinivas M.
    J Chromatogr Sci; 2013 Mar; 51(3):215-21. PubMed ID: 22865837
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  • 27. A validated stability-indicating normal phase LC method for clopidogrel bisulfate and its impurities in bulk drug and pharmaceutical dosage form.
    Durga Rao D, Kalyanaraman L, Sait SS, Venkata Rao P.
    J Pharm Biomed Anal; 2010 May 01; 52(1):160-5. PubMed ID: 20074888
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  • 29. Quality by design approach for the separation of naproxcinod and its related substances by fused core particle technology column.
    Inugala UR, Pothuraju NR, Vangala RR.
    J Chromatogr Sci; 2013 May 01; 51(5):453-9. PubMed ID: 23060406
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  • 35. Development and Validation of a Stability-Indicating RP-UPLC Method for the Estimation of Impurities in Cinacalcet Hydrochloride API and its Formulation.
    Sunil Reddy P, Raju TV, Raju PS, Varma NS, Babu KS.
    Sci Pharm; 2015 May 01; 83(4):583-98. PubMed ID: 26839840
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  • 37. Stability-indicating liquid chromatographic method for determination of saxagliptin and structure elucidation of the major degradation products using LC-MS.
    Abdel-Ghany MF, Abdel-Aziz O, Ayad MF, Tadros MM.
    J Chromatogr Sci; 2015 Apr 01; 53(4):554-64. PubMed ID: 25060753
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  • 40. Development and Validation of a Stability-Indicating RP-HPLC Method for the Determination of Process-Related Impurities and Degradation Products of Rabeprazole Sodium in Pharmaceutical Formulation.
    Kumar N, Sangeetha D.
    Sci Pharm; 2013 Apr 01; 81(3):697-711. PubMed ID: 24106668
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