453 related articles for article (PubMed ID: 18771002)
1. 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; 63(8):562-7. PubMed ID: 18771002
[TBL] [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; 52(3):362-71. PubMed ID: 19926421
[TBL] [Abstract][Full Text] [Related]
3. Development and validation of a HPLC method for the determination of buprenorphine hydrochloride, naloxone hydrochloride and noroxymorphone in a tablet formulation.
Mostafavi A; Abedi G; Jamshidi A; Afzali D; Talebi M
Talanta; 2009 Feb; 77(4):1415-9. PubMed ID: 19084658
[TBL] [Abstract][Full Text] [Related]
4. 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; 46(2):295-302. PubMed ID: 18054459
[TBL] [Abstract][Full Text] [Related]
5. Simple and reliable HPLC analysis of fexofenadine hydrochloride in tablets and its application to dissolution studies.
Oliveira DC; Weigch A; Rolim CM
Pharmazie; 2007 Feb; 62(2):96-100. PubMed ID: 17341026
[TBL] [Abstract][Full Text] [Related]
6. Development and validation of a stability-indicating high performance liquid chromatographic (HPLC) assay for biperiden in bulk form and pharmaceutical dosage forms.
Mohammadi A; Mehramizi A; Moghaddam FA; Jabarian LE; Pourfarzib M; Kashani HN
J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Jul; 854(1-2):152-7. PubMed ID: 17466605
[TBL] [Abstract][Full Text] [Related]
7. Development and validation of a reversed-phase HPLC method for simultaneous estimation of ambroxol hydrochloride and azithromycin in tablet dosage form.
Shaikh KA; Patil SD; Devkhile AB
J Pharm Biomed Anal; 2008 Dec; 48(5):1481-4. PubMed ID: 18993009
[TBL] [Abstract][Full Text] [Related]
8. Validated stability-indicating HPLC method for the determination of dimethyl-4,4'-dimethoxy-5,6,5',6'-dimethylene dioxybiphenyl-2,2'-dicarboxylate (DDB) and its degradation products.
Hadad GM
J Pharm Biomed Anal; 2008 Aug; 47(4-5):695-703. PubMed ID: 18403161
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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; 36(2):341-50. PubMed ID: 15496327
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Development and validation of a HPLC-UV method for the determination in didanosine tablets.
de Oliveira AM; Löwen TC; Cabral LM; dos Santos EM; Rodrigues CR; Castro HC; dos Santos TC
J Pharm Biomed Anal; 2005 Jul; 38(4):751-6. PubMed ID: 15967304
[TBL] [Abstract][Full Text] [Related]
13. A stability-indicating high performance liquid chromatographic assay for the determination of orlistat in capsules.
Mohammadi A; Haririan I; Rezanour N; Ghiasi L; Walker RB
J Chromatogr A; 2006 May; 1116(1-2):153-7. PubMed ID: 16603170
[TBL] [Abstract][Full Text] [Related]
14. Development and validation of a stability-indicating HPLC-UV method for the determination of alizapride and its degradation products.
Tamaro I; Aprile S; Giovenzana GB; Grosa G
J Pharm Biomed Anal; 2010 Apr; 51(5):1024-31. PubMed ID: 19962264
[TBL] [Abstract][Full Text] [Related]
15. A stability-indicating high performance liquid chromatographic (HPLC) assay for the simultaneous determination of atorvastatin and amlodipine in commercial tablets.
Mohammadi A; Rezanour N; Ansari Dogaheh M; Ghorbani Bidkorbeh F; Hashem M; Walker RB
J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Feb; 846(1-2):215-21. PubMed ID: 17010681
[TBL] [Abstract][Full Text] [Related]
16. 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; 43(3):873-8. PubMed ID: 17023136
[TBL] [Abstract][Full Text] [Related]
17. Development and validation of a high-performance liquid chromatographic method for the analysis of budesonide.
Gupta M; Bhargava HN
J Pharm Biomed Anal; 2006 Feb; 40(2):423-8. PubMed ID: 16143482
[TBL] [Abstract][Full Text] [Related]
18. 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; 57(5):313-5. PubMed ID: 12061254
[TBL] [Abstract][Full Text] [Related]
19. Development and application of a validated stability-indicating HPLC method for simultaneous determination of granisetron hydrochloride, benzyl alcohol and their main degradation products in parenteral dosage forms.
Hewala I; El-Fatatre H; Emam E; Mubrouk M
Talanta; 2010 Jun; 82(1):184-95. PubMed ID: 20685455
[TBL] [Abstract][Full Text] [Related]
20. Fesoterodine stress degradation behavior by liquid chromatography coupled to ultraviolet detection and electrospray ionization mass spectrometry.
Sangoi MS; Todeschini V; Steppe M
Talanta; 2011 May; 84(4):1068-79. PubMed ID: 21530781
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]