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