62 related articles for article (PubMed ID: 3980423)
1. Validation of liquid chromatographic method for assay of chlorthalidone in tablet formulations.
Fogel J; Sisco J; Hess F
J Assoc Off Anal Chem; 1985; 68(1):96-8. PubMed ID: 3980423
[TBL] [Abstract][Full Text] [Related]
2. Liquid chromatographic method for identity, assay, and content uniformity of five tricyclic drugs.
Lovering EG; Beaulieu N; Lawrence RC; Sears RW
J Assoc Off Anal Chem; 1985; 68(2):168-71. PubMed ID: 2859267
[TBL] [Abstract][Full Text] [Related]
3. Stability-indicating assay for chlorthalidone formulation: evaluation of the USP analysis and a high-performance liquid chromatographic analysis.
Bauer J; Quick J; Krogh S; Shada D
J Pharm Sci; 1983 Aug; 72(8):924-8. PubMed ID: 6620149
[TBL] [Abstract][Full Text] [Related]
4. Determination of inorganic nitrate impurity from nicorandil and its tablet dosage form by simple reversed phase liquid chromatographic method.
Mehta TN; Gadhvi MP; Subbaiah G
J Chromatogr A; 2006 Jan; 1101(1-2):153-7. PubMed ID: 16236291
[TBL] [Abstract][Full Text] [Related]
5. High performance liquid chromatographic determination of clotrimazole in pharmaceutical formulations.
Hoogerheide JG; Strusiak SH; Taddei CR; Townley ER; Wyka BE
J Assoc Off Anal Chem; 1981 Jul; 64(4):864-9. PubMed ID: 7275902
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Liquid chromatographic determination of methocarbamol in injection and tablet dosage forms: collaborative study.
Everett RL
J Assoc Off Anal Chem; 1984; 67(2):225-7. PubMed ID: 6725189
[TBL] [Abstract][Full Text] [Related]
8. Determination of chlorthalidone and clonidine hydrochloride in tablets by HPLC.
Walters SM; Stonys DB
J Chromatogr Sci; 1983 Jan; 21(1):43-5. PubMed ID: 6833444
[TBL] [Abstract][Full Text] [Related]
9. Liquid chromatographic determination of prednisolone in tablets and bulk drugs: interlaboratory study.
Brower JF
J Assoc Off Anal Chem; 1984; 67(4):674-6. PubMed ID: 6469892
[TBL] [Abstract][Full Text] [Related]
10. Quantitative determination of chlorthalidone in pharmaceutical dosage forms by high-pressure liquid chromatography.
O'Hare MJ; Tan E; Moody JE
J Pharm Sci; 1979 Jan; 68(1):106-8. PubMed ID: 758442
[TBL] [Abstract][Full Text] [Related]
11. Liquid chromatographic determination of hydrocortisone in bulk drug substance and tablets: collaborative study.
Walters MJ
J Assoc Off Anal Chem; 1984; 67(2):218-21. PubMed ID: 6725187
[TBL] [Abstract][Full Text] [Related]
12. Reverse phase liquid chromatographic determination of bisacodyl in dosage forms.
Valenti LP; Lau-Cam CA
J Assoc Off Anal Chem; 1985; 68(3):529-32. PubMed ID: 4019380
[TBL] [Abstract][Full Text] [Related]
13. LC and LC-MS/MS study of forced decomposition behavior of anastrozole and establishment of validated stability-indicating analytical method for impurities estimation in low dose anastrozole tablets.
Reddy YR; Nandan SR; Bharathi DV; Nagaraju B; Reddy SS; Ravindranath LK; Rao VS
J Pharm Biomed Anal; 2009 Oct; 50(3):397-404. PubMed ID: 19541446
[TBL] [Abstract][Full Text] [Related]
14. LC and LC-MS study of stress decomposition behaviour of isoniazid and establishment of validated stability-indicating assay method.
Bhutani H; Singh S; Vir S; Bhutani KK; Kumar R; Chakraborti AK; Jindal KC
J Pharm Biomed Anal; 2007 Mar; 43(4):1213-20. PubMed ID: 17118610
[TBL] [Abstract][Full Text] [Related]
15. Thin layer densitometry in the quantitative assay of drugs. Note V--Assay of reserpine and chlorthalidone in the presence of the potential impurities of their solid pharmaceutical forms.
Corti P; Corbini G; Dreassi E; Murratzu C; Celesti L
Pharm Acta Helv; 1990; 65(8):222-7. PubMed ID: 2236179
[TBL] [Abstract][Full Text] [Related]
16. Study of forced degradation behavior of eletriptan hydrobromide by LC and LC-MS and development of stability-indicating method.
Jocić B; Zecević M; Zivanović L; Protić A; Jadranin M; Vajs V
J Pharm Biomed Anal; 2009 Nov; 50(4):622-9. PubMed ID: 19250786
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A stability indicating LC method for zolmitriptan.
Rao BM; Srinivasu MK; Sridhar G; Kumar PR; Chandrasekhar KB; Islam A
J Pharm Biomed Anal; 2005 Sep; 39(3-4):503-9. PubMed ID: 15899567
[TBL] [Abstract][Full Text] [Related]
19. Reverse phase high performance liquid chromatographic determination of phenprocoumon in tablets.
Schmidt WF
J Assoc Off Anal Chem; 1982 May; 65(3):753-5. PubMed ID: 7096256
[TBL] [Abstract][Full Text] [Related]
20. Validation of a fast liquid chromatography-UV method for the analysis of drugs used in combined cardiovascular therapy in human plasma.
Iriarte G; Gonzalez O; Ferreirós N; Maguregui MI; Alonso RM; Jiménez RM
J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Oct; 877(27):3045-53. PubMed ID: 19660995
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]