Development and validation of stability indicating RP-HPLC method for the simultaneous estimation of Sofosbuvir and Ledipasvir in bulk and their combined dosage form-Reference-Cited by-同舟云学术

Development and validation of stability indicating RP-HPLC method for the simultaneous estimation of Sofosbuvir and Ledipasvir in bulk and their combined dosage form

Published:2018-12 Issue:2 Volume:4 Page:116-123
ISSN:2314-7245
Container-title:Future Journal of Pharmaceutical Sciences
language:en
Short-container-title:Future Journal of Pharmaceutical Sciences

Author:

Mastanamma S.K.,Chandini S.K.,Reehana S.K.,Saidulu P.

Publisher

Springer Science and Business Media LLC

Reference7 articles.

1. Available from: https://www.drugbank.ca/drugs/DB08934.

2. Available from: https://www.drugbank.ca/drugs/DB09027.

3. Method development and validation of new RP- HPLC method for the determination of sofosbuvir in pure form;Mohan Vikas;World J. Pharm. Pharmaceut. Sci.,2016

4. Estimation and validation of sofosbuvir in bulk and tablet dosage form;Vejendlal;Int. J. Pharm.,2016

5. Method development and validation of new RP- HPLC method for the determination of sofosbuvir tablet;Guguloth;J. Pharma Res.,2016

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