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177 related items for PubMed ID: 25487685
1. Determination of stress-induced degradation products of cetirizine dihydrochloride by a stability-indicating RP-HPLC method. Flórez Borges P, Pérez Lozano P, García Montoya E, Miñarro M, Ticó JR, Jo E, Suñe Negre JM. Daru; 2014 Dec 09; 22(1):82. PubMed ID: 25487685 [Abstract] [Full Text] [Related]
2. 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]
3. Development and validation of a stability indicating RP-HPLC method for the simultaneous determination of related substances of albuterol sulfate and ipratropium bromide in nasal solution. Kasawar GB, Farooqui M. J Pharm Biomed Anal; 2010 May 01; 52(1):19-29. PubMed ID: 20045275 [Abstract] [Full Text] [Related]
4. Determination of cetirizine dihydrochloride, related impurities and preservatives in oral solution and tablet dosage forms using HPLC. Jaber AM, Al Sherife HA, Al Omari MM, Badwan AA. J Pharm Biomed Anal; 2004 Oct 29; 36(2):341-50. PubMed ID: 15496327 [Abstract] [Full Text] [Related]
5. Development and validation of a rapid RP-HPLC method for the determination of cetirizine or fexofenadine with pseudoephedrine in binary pharmaceutical dosage forms. Karakuş S, Küçükgüzel I, Küçükgüzel SG. J Pharm Biomed Anal; 2008 Jan 22; 46(2):295-302. PubMed ID: 18054459 [Abstract] [Full Text] [Related]
6. Preparation and characterization of two new forced degradation products of letrozole and development of a stability-indicating RP-LC method for its determination. Elkady EF, Fouad MA. Pak J Pharm Sci; 2015 Nov 22; 28(6):2041-51. PubMed ID: 26639498 [Abstract] [Full Text] [Related]
7. Enantioselective determination of cetirizine in human plasma by normal-phase liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry. Kang SW, Jang HJ, Moore VS, Park JY, Kim KA, Youm JR, Han SB. J Chromatogr B Analyt Technol Biomed Life Sci; 2010 Dec 15; 878(32):3351-7. PubMed ID: 21081290 [Abstract] [Full Text] [Related]
8. Development and validation of a HPLC method for the analysis of promethazine hydrochloride in hot-melt extruded dosage forms. Thumma S, Zhang SQ, Repka MA. Pharmazie; 2008 Aug 15; 63(8):562-7. PubMed ID: 18771002 [Abstract] [Full Text] [Related]
9. STABILITY-INDICATING HPLC METHOD FOR DETERMINATION OF VANCOMYCIN HYDROCHLORIDE IN THE PHARMACEUTICAL DOSAGE FORMS. Serri A, Moghimp HR, Mahboubi A, Zarghi A. Acta Pol Pharm; 2017 Jan 15; 74(1):73-79. PubMed ID: 29474763 [Abstract] [Full Text] [Related]
10. RP-HPLC stability-indicating assay method for talinolol and characterization of its degradation products. Sinha VR, Ghai D. J Chromatogr Sci; 2011 Jan 15; 49(10):786-95. PubMed ID: 22080807 [Abstract] [Full Text] [Related]
11. 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 15; 50(9):810-9. PubMed ID: 22661461 [Abstract] [Full Text] [Related]
12. A validated stability-indicating HPLC method for the simultaneous determination of pheniramine maleate and naphazoline hydrochloride in pharmaceutical formulations. Huang T, Chen N, Wang D, Lai Y, Cao Z. Chem Cent J; 2014 Feb 01; 8(1):7. PubMed ID: 24485011 [Abstract] [Full Text] [Related]
13. Development of a stability-indicating HPLC method of etifoxine with characterization of degradation products by LC-MS/TOF, 1H and 13C NMR. Djabrouhou N, Guermouche MH. J Pharm Biomed Anal; 2014 Nov 01; 100():11-20. PubMed ID: 25117950 [Abstract] [Full Text] [Related]
14. Validation of HPLC-UV Assay of Caffeic Acid in Emulsions. Spagnol CM, Isaac VL, Corrêa MA, Salgado HR. J Chromatogr Sci; 2016 Mar 01; 54(3):305-11. PubMed ID: 26499121 [Abstract] [Full Text] [Related]
15. Method development and validation for the simultaneous determination of cetirizine dihydrochloride, paracetamol, and phenylpropanolamine hydrochloride in tablets by capillary zone electrophoresis. Azhagvuel S, Sekar R. J Pharm Biomed Anal; 2007 Feb 19; 43(3):873-8. PubMed ID: 17023136 [Abstract] [Full Text] [Related]
16. A validated stability indicating RP-HPLC method for estimation of Armodafinil in pharmaceutical dosage forms and characterization of its base hydrolytic product. Venkateswarlu K, Rangareddy A, Narasimhaiah K, Sharma H, Bandi NMR. Pak J Pharm Sci; 2017 Jan 19; 30(1):23-28. PubMed ID: 28603108 [Abstract] [Full Text] [Related]
17. Stability-indicating RP-LC method for determination of azilsartan medoxomil and chlorthalidone in pharmaceutical dosage forms: application to degradation kinetics. Ebeid WM, Elkady EF, El-Zaher AA, El-Bagary RI, Patonay G. Anal Bioanal Chem; 2014 Oct 19; 406(26):6701-12. PubMed ID: 25190009 [Abstract] [Full Text] [Related]
18. Development and validation of stability-indicating HPLC method for determination of cefpirome sulfate. Zalewski P, Skibiński R, Cielecka-Piontek J, Bednarek-Rajewska K. Acta Pol Pharm; 2014 Oct 19; 71(5):731-6. PubMed ID: 25362801 [Abstract] [Full Text] [Related]
19. Determination of progesterone (steroid drug) in the semi-solid dosage form (vaginal gel) using a stability-indicating method by RP-HPLC/PDA detector. Konduru N, Kethe VB, Gundla R, Katari NK, Mallavarapu R. Biomed Chromatogr; 2022 Jan 19; 36(1):e5246. PubMed ID: 34523747 [Abstract] [Full Text] [Related]
20. Development and validation of a HPLC method for the determination of cetirizine in pharmaceutical dosage forms. Paw B, Misztal G, Hopkała H, Drozd J. Pharmazie; 2002 May 19; 57(5):313-5. PubMed ID: 12061254 [Abstract] [Full Text] [Related] Page: [Next] [New Search]