177 related articles for article (PubMed ID: 15351048)
1. Development and validation of a fully automated method for the chromatographic determination of content uniformity of drug tablets.
Toro I; Dulsat JF; Fábregas JL; Claramunt J
J Pharm Biomed Anal; 2004 Sep; 36(1):57-63. PubMed ID: 15351048
[TBL] [Abstract][Full Text] [Related]
2. Development and validation of a reversed-phase liquid chromatographic method for analysis of degradation products of estradiol in Vagifem tablets.
Nygaard L; Drøhse Kilde H; Andersen SG; Henriksen L; Overby V
J Pharm Biomed Anal; 2004 Feb; 34(2):265-76. PubMed ID: 15013140
[TBL] [Abstract][Full Text] [Related]
3. Development and validation of a new HPLC analytical method for the determination of alprazolam in tablets.
Pérez-Lozano P; García-Montoya E; Orriols A; Miñarro M; Ticó JR; Suñé-Negre JM
J Pharm Biomed Anal; 2004 Mar; 34(5):979-87. PubMed ID: 15019032
[TBL] [Abstract][Full Text] [Related]
4. Development and validation of a gradient HPLC method for the determination of clindamycin and related compounds in a novel tablet formulation.
Platzer DJ; White BA
J Pharm Biomed Anal; 2006 Apr; 41(1):84-8. PubMed ID: 16298506
[TBL] [Abstract][Full Text] [Related]
5. Development and validation of an analytical method for metformin hydrochloride and its related compound (1-cyanoguanidine) in tablet formulations by HPLC-UV.
Al-Rimawi F
Talanta; 2009 Oct; 79(5):1368-71. PubMed ID: 19635372
[TBL] [Abstract][Full Text] [Related]
6. Validation of a dissolution method with HPLC analysis for lasofoxifene tartrate low dose tablets.
Space JS; Opio AM; Nickerson B; Jiang H; Dumont M; Berry M
J Pharm Biomed Anal; 2007 Sep; 44(5):1064-71. PubMed ID: 17560750
[TBL] [Abstract][Full Text] [Related]
7. Development and validation of RP-HPLC and ultraviolet spectrophotometric methods of analysis for the quantitative estimation of antiretroviral drugs in pharmaceutical dosage forms.
Sarkar M; Khandavilli S; Panchagnula R
J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Jan; 830(2):349-54. PubMed ID: 16330261
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Development and validation of a new gas flame ionization detector method for the determination of finasteride in tablets.
Sağlik S; Tatar Ulu S
Anal Biochem; 2006 May; 352(2):260-4. PubMed ID: 16527234
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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; 46(2):236-42. PubMed ID: 18029132
[TBL] [Abstract][Full Text] [Related]
12. Application of stability-indicating HPTLC method for quantitative determination of metadoxine in pharmaceutical dosage form.
Kaul N; Agrawal H; Patil B; Kakad A; Dhaneshwar SR
Farmaco; 2005 Apr; 60(4):351-60. PubMed ID: 15848212
[TBL] [Abstract][Full Text] [Related]
13. Automated 96-well solid phase extraction and hydrophilic interaction liquid chromatography-tandem mass spectrometric method for the analysis of cetirizine (ZYRTEC) in human plasma--with emphasis on method ruggedness.
Song Q; Junga H; Tang Y; Li AC; Addison T; McCort-Tipton M; Beato B; Naidong W
J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Jan; 814(1):105-14. PubMed ID: 15607714
[TBL] [Abstract][Full Text] [Related]
14. Gradient HPLC analysis of raloxifene hydrochloride and its application to drug quality control.
Basavaiah K; Anil Kumar UR; Tharpa K
Acta Pharm; 2008 Sep; 58(3):347-56. PubMed ID: 19103571
[TBL] [Abstract][Full Text] [Related]
15. Automated determination of flutamide by a validated flow-injection method: application to dissolution studies of pharmaceutical tablets.
Tzanavaras PD; Themelis DG
J Pharm Biomed Anal; 2007 Apr; 43(5):1820-4. PubMed ID: 17197148
[TBL] [Abstract][Full Text] [Related]
16. Automated sample preparation of Roxifiban tablets: transfer of a manual method to an automated workstation.
Shamrock WF; Reilly K; Lloyd DK
J Pharm Biomed Anal; 2000 Jan; 21(6):1225-32. PubMed ID: 10708406
[TBL] [Abstract][Full Text] [Related]
17. Simultaneous determination of pioglitazone and glimepiride in bulk drug and pharmaceutical dosage form by RP-HPLC method.
A K; G S; C MR; Bhat K; A R; P M; M S; K K; N U
Pak J Pharm Sci; 2008 Oct; 21(4):421-5. PubMed ID: 18930865
[TBL] [Abstract][Full Text] [Related]
18. Validation of direct assay of an aqueous formulation of a drug compound AZY by chiral supercritical fluid chromatography (SFC).
Mukherjee PS
J Pharm Biomed Anal; 2007 Jan; 43(2):464-70. PubMed ID: 16930907
[TBL] [Abstract][Full Text] [Related]
19. Development and validation of RP-HPLC method to determine letrozole in different pharmaceutical formulations and its application to studies of drug release from nanoparticles.
Mondal N; Pal TK; Ghosal SK
Acta Pol Pharm; 2009; 66(1):11-7. PubMed ID: 19226963
[TBL] [Abstract][Full Text] [Related]
20. On-line coupling of sequential injection with liquid chromatography for the automated derivatization and determination of gamma-aminobutyric acid in human biological fluids.
Zacharis CK; Theodoridis GA; Voulgaropoulos AN
J Chromatogr B Analyt Technol Biomed Life Sci; 2004 Sep; 808(2):169-75. PubMed ID: 15261810
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
