These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
225 related articles for article (PubMed ID: 25176232)
1. Development and validation of HPLC analytical method for nepafenac in ophthalmic dosage form (suspension). Usman S; Akram M; Aziz A; Ramesh V; Sarheed OA Pak J Pharm Sci; 2014 Sep; 27(5 Spec no):1541-6. PubMed ID: 25176232 [TBL] [Abstract][Full Text] [Related]
2. Development and validation of RP HPLC method to determine nandrolone phenylpropionate in different pharmaceutical formulations. Mukherjee J; Das A; Chakrabarty US; Sahoo BK; Dey G; Choudhury H; Pal TK Acta Pol Pharm; 2011; 68(2):155-60. PubMed ID: 21485287 [TBL] [Abstract][Full Text] [Related]
3. 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; 52(3):362-71. PubMed ID: 19926421 [TBL] [Abstract][Full Text] [Related]
4. Investigation of the spectrofluorimetric behavior of azelastine and nepafenac: Determination in ophthalmic dosage forms. Ragab MAA; El-Kimary EI Spectrochim Acta A Mol Biomol Spectrosc; 2018 Nov; 204():260-266. PubMed ID: 29936223 [TBL] [Abstract][Full Text] [Related]
5. Determination of organic volatile impurities in nepafenac by GC method. Mucha M; Groman A; Zagrodzka J; Cybulski M Acta Pol Pharm; 2014; 71(6):1013-22. PubMed ID: 25745773 [TBL] [Abstract][Full Text] [Related]
6. Determination of Cefadroxil in Tablet/Capsule formulations by a validated Reverse Phase High Performance Liquid Chromatographic method. Rahim N; Naqvi SB; Shakeel S; Iffat W; Muhammad IN Pak J Pharm Sci; 2015 Jul; 28(4):1345-9. PubMed ID: 26142506 [TBL] [Abstract][Full Text] [Related]
7. Development and validation of high performance liquid chromatography with a spectrophotometric detection method for the chemical purity and assay of nepafenac. Lipiec-Abramska E; Jedynak Ł; Formela A; Roszczyński J; Cybulski M; Puchalska M; Zagrodzka J J Pharm Biomed Anal; 2014 Mar; 91():1-6. PubMed ID: 24406462 [TBL] [Abstract][Full Text] [Related]
8. Forced degradation of nepafenac: Development and validation of stability indicating UHPLC method. Runje M; Babić S; Meštrović E; Nekola I; Dujmić-Vučinić Ž; Vojčić N J Pharm Biomed Anal; 2016 May; 123():42-52. PubMed ID: 26871279 [TBL] [Abstract][Full Text] [Related]
9. Validated RP-HPLC/UV method for the quantitation of abiraterone in rat plasma and its application to a pharmacokinetic study in rats. Kumar SV; Rudresha G; Gurav S; Zainuddin M; Dewang P; Kethiri RR; Rajagopal S; Mullangi R Biomed Chromatogr; 2013 Feb; 27(2):203-7. PubMed ID: 22763809 [TBL] [Abstract][Full Text] [Related]
10. 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; 52(1):19-29. PubMed ID: 20045275 [TBL] [Abstract][Full Text] [Related]
11. Comparison of the analgesic efficacy and safety of nepafenac ophthalmic suspension compared with diclofenac ophthalmic solution for ocular pain and photophobia after excimer laser surgery: a phase II, randomized, double-masked trial. Colin J; Paquette B Clin Ther; 2006 Apr; 28(4):527-36. PubMed ID: 16750464 [TBL] [Abstract][Full Text] [Related]
13. Development and validation of a novel RP-HPLC method for the analysis of reduced glutathione. Sutariya V; Wehrung D; Geldenhuys WJ J Chromatogr Sci; 2012 Mar; 50(3):271-6. PubMed ID: 22337804 [TBL] [Abstract][Full Text] [Related]
15. 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; 360(1-2):77-82. PubMed ID: 18524511 [TBL] [Abstract][Full Text] [Related]
16. Simultaneous quantitation of aspirin, amlodipine and simvastatin in a fixed dose combination of encapsulated tablet formulation by HPLC-UV method. Sultan F; Shoaib MH; Yousuf RI; Ahmed FR; Salam FA; Nasiri MI; Khan MA; Manzoor S Pak J Pharm Sci; 2014 Sep; 27(5 Spec no):1553-8. PubMed ID: 25176250 [TBL] [Abstract][Full Text] [Related]
17. Development and validation of a simple reversed-phase HPLC method for the determination of camptothecin in animal organs following administration in solid lipid nanoparticles. Martins SM; Wendling T; Gonçalves VM; Sarmento B; Ferreira DC J Chromatogr B Analyt Technol Biomed Life Sci; 2012 Jan; 880(1):100-7. PubMed ID: 22153332 [TBL] [Abstract][Full Text] [Related]
18. A stability-indicating HPLC method for the determination of glucosamine in pharmaceutical formulations. Shao Y; Alluri R; Mummert M; Koetter U; Lech S J Pharm Biomed Anal; 2004 May; 35(3):625-31. PubMed ID: 15137989 [TBL] [Abstract][Full Text] [Related]
19. Use of chemometrics for development and validation of an RP-HPLC method for simultaneous determination of haloperidol and related compounds. Petkovska R; Dimitrovska A Acta Pharm; 2008 Sep; 58(3):243-56. PubMed ID: 19103562 [TBL] [Abstract][Full Text] [Related]
20. Validation and application of reversed phase high-performance liquid chromatographic method for quantification of pizotifen malate in pharmaceutical solid dosage formulations. Rahman SM; Lutfulkabir A; Jahan MD; Momen AZ; Rouf AS Pak J Pharm Sci; 2010 Oct; 23(4):435-41. PubMed ID: 20884459 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]