Development and validation of a new stability indicating RP-HPLC method for the quantification of Budesonide in pharmaceutical dosage forms in presence of an internal standard

Bandaru Sai Pavan Kumar; Mukthinuthalapati Mathrusri Annapurna

doi:10.52711/0974-360X.2022.00349

Research Journal of Pharmacy and Technology

ISSN

0974-360X (Online)
0974-3618 (Print)

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Development and validation of a new stability indicating RP-HPLC method for the quantification of Budesonide in pharmaceutical dosage forms in presence of an internal standard

Author(s): Bandaru Sai Pavan Kumar, Mukthinuthalapati Mathrusri Annapurna

Email(s): mmukthin@gitam.edu

DOI: 10.52711/0974-360X.2022.00349

Address: Bandaru Sai Pavan Kumar, Mukthinuthalapati Mathrusri Annapurna*
Department of Pharmaceutical Analysis, GITAM Institute of Pharmacy, Gandhi Institute of Technology and Management (Deemed to be University), Visakhapatnam, Andhra Pradesh-530045, India.
*Corresponding Author

Published In: Volume - 15, Issue - 5, Year - 2022

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Cite this article:
Bandaru Sai Pavan Kumar, Mukthinuthalapati Mathrusri Annapurna. Development and validation of a new stability indicating RP-HPLC method for the quantification of Budesonide in pharmaceutical dosage forms in presence of an internal standard. Research Journal of Pharmacy and Technology. 2022; 15(5):2103-9. doi: 10.52711/0974-360X.2022.00349

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