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Journal Abstract Search

198 related items for PubMed ID: 22298755

  • 1. Development and validation of a stability-indicating RP-UPLC method for the quantitative analysis of nabumetone in tablet dosage form.
    Sethi N, Anand A, Chandrul KK, Jain G, Srinivas KS.
    J Chromatogr Sci; 2012 Feb; 50(2):85-90. PubMed ID: 22298755
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  • 2. 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
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  • 3. Development and validation of a stability-indicating RP-UPLC method for the quantitative analysis of sparfloxacin.
    Gupta H, Aqil M, Khar RK, Ali A, Sharma A, Chander P.
    J Chromatogr Sci; 2010 Jan 22; 48(1):1-6. PubMed ID: 20056027
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  • 4. 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 22; 50(9):810-9. PubMed ID: 22661461
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  • 9. Development of a stability-indicating UPLC method for determining olanzapine and its associated degradation products present in active pharmaceutical ingredients and pharmaceutical dosage forms.
    Krishnaiah Ch, Vishnu Murthy M, Kumar R, Mukkanti K.
    J Pharm Biomed Anal; 2011 Mar 25; 54(4):667-73. PubMed ID: 21075576
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  • 12. Stability-indicating LC method for the simultaneous determination of lisinopril and hydrochlorothiazide.
    de Diego M, Soto J, Mennickent S.
    J Chromatogr Sci; 2014 Mar 25; 52(10):1193-7. PubMed ID: 24297524
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  • 14. Validation and method development of Tadalafil in bulk and tablet dosage form by RP-HPLC.
    Bojanapu A, Subramaniam AT, Munusamy J, Dhanapal K, Chennakesavalu J, Sellappan M, Jayaprakash V.
    Drug Res (Stuttg); 2015 Feb 25; 65(2):82-5. PubMed ID: 24782284
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  • 16. A New Rapid and Sensitive Stability-Indicating UPLC Assay Method for Tolterodine Tartrate: Application in Pharmaceuticals, Human Plasma and Urine Samples.
    Yanamandra R, Vadla CS, Puppala U, Patro B, Murthy YL, Ramaiah PA.
    Sci Pharm; 2012 Feb 25; 80(1):101-14. PubMed ID: 22396907
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  • 17. Development and validation of a reversed-phase HPLC method for simultaneous analysis of butylhydroxyanisol, simvastatin and its impurities in tablet dosage forms.
    El Karbane M, Azougagh M, Amood A L-Kamarany M, Bouchafra H, Cherrah Y, Bouklouze A.
    Ann Pharm Fr; 2014 Jul 25; 72(4):244-55. PubMed ID: 24997886
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  • 18. 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 25; 52(7):609-16. PubMed ID: 23825352
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  • 20. Stability-indicating UPLC method for determination of Imatinib Mesylate and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms.
    Nageswari A, Reddy KV, Mukkanti K.
    J Pharm Biomed Anal; 2012 Jul 25; 66():109-15. PubMed ID: 22502910
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