Author(s): Devshree Yashwantbhai Patel, Javesh Kashinath Patil, Harsha Vasudev Chaudhari, Ruchita M Kothari

Email(s): devshree744@gmail.com

DOI: 10.52711/2231-5675.2024.00038

Address: Devshree Yashwantbhai Patel1, Javesh Kashinath Patil2, Harsha Vasudev Chaudhari3, Ruchita M Kothari4
1Department of Pharmaceutical Quality Assurance, P.S.G.V.P. Mandal’s College of Pharmacy, Shahada, Dist - Nandurbar, 425409, Maharashtra, India.
2Associate Professor, Department of Pharmaceutical Quality Assurance, P.S.G.V.P. Mandal’s College of Pharmacy, Shahada, Dist. - Nandurbar, 425409, Maharashtra, India.
3Department of Pharmaceutical Quality Assurance, P.S.G.V.P. Mandal’s College of Pharmacy, Shahada, Dist - Nandurbar, 425409, Maharashtra, India.
4Department of Pharmaceutical Quality Assurance, P.S.G.V.P. Mandal’s College of Pharmacy, Shahada, Dist - Nandurbar, 425409, India.
*Corresponding Author

Published In:   Volume - 14,      Issue - 4,     Year - 2024


Cite this article:
Devshree Yashwantbhai Patel, Javesh Kashinath Patil, Harsha Vasudev Chaudhari, Ruchita M Kothari. Analytical Method Development and Validation of Nitazoxanide by RP-HPLC Method in API and Tablet Dosage Forms. Asian Journal of Pharmaceutical Analysis. 2024; 14(4):211-6. doi: 10.52711/2231-5675.2024.00038




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