Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 6

1.

Quantification of halobetasol propionate and its impurities present in topical dosage forms by stability-indicating LC method.

Nalwade S, Reddy VR, Kulkarni D, Todamal S.

J Chromatogr Sci. 2015 Jan;53(1):127-34. doi: 10.1093/chromsci/bmu029. Epub 2014 Apr 30.

PMID:
24784115
2.

Stability-indicating UPLC method for determining related substances and degradants in dronedarone.

Pydimarry SP, Cholleti VK, Vangala RR.

J Chromatogr Sci. 2014 Aug;52(7):666-75. doi: 10.1093/chromsci/bmt097. Epub 2013 Jul 17.

PMID:
23863770
3.

A validated stability-indicating liquid chromatographic method for the determination of retapamulin in topical dosage form.

Nalwade S, Reddy VR.

J Chromatogr Sci. 2014 Mar;52(3):238-45. doi: 10.1093/chromsci/bmt018. Epub 2013 Mar 19.

PMID:
23510782
4.

Quality by design approach for the separation of naproxcinod and its related substances by fused core particle technology column.

Inugala UR, Pothuraju NR, Vangala RR.

J Chromatogr Sci. 2013 May-Jun;51(5):453-9. doi: 10.1093/chromsci/bms162. Epub 2012 Oct 11.

PMID:
23060406
5.

A validated stability indicating ultra performance liquid chromatographic method for determination of impurities in Esomeprazole magnesium gastro resistant tablets.

Nalwade SU, Reddy VR, Rao DD, Morisetti NK.

J Pharm Biomed Anal. 2012 Jan 5;57:109-14. doi: 10.1016/j.jpba.2011.08.025. Epub 2011 Aug 22.

PMID:
21920688
6.

Rapid simultaneous determination of telmisartan, amlodipine besylate and hydrochlorothiazide in a combined poly pill dosage form by stability-indicating ultra performance liquid chromatography.

Nalwade S, Ranga Reddy V, Durga Rao D, Koteswara Rao I.

Sci Pharm. 2011 Jan-Mar;79(1):69-84. doi: 10.3797/scipharm.1006-10. Epub 2011 Jan 4.

Supplemental Content

Loading ...
Support Center