Stability Indicating Assay for the Determination of Bilastine in Bulk Drug and Method Development Validation by RP-HPLC Using Analytical Quality by Design Approaches.

MLA

Nayak, Anjali, et al. “Stability Indicating Assay for the Determination of Bilastine in Bulk Drug and Method Development Validation by RP-HPLC Using Analytical Quality by Design Approaches.” Indian Journal of Pharmaceutical Education & Research, vol. 58, Apr. 2024, pp. S582–90. EBSCOhost, https://doi.org/10.5530/ijper.58.2s.61.

APA

Nayak, A., Alwin, R. M. D., G., S., C. Y., S., Reddy, Y. V., & Dang, R. (2024). Stability Indicating Assay for the Determination of Bilastine in Bulk Drug and Method Development Validation by RP-HPLC Using Analytical Quality by Design Approaches. Indian Journal of Pharmaceutical Education & Research, 58, S582–S590. https://doi.org/10.5530/ijper.58.2s.61

Chicago

Nayak, Anjali, R. Maria Danish Alwin, Sangeetha G., Sowmya C. Y., Yashwanth V. Reddy, and Raman Dang. 2024. “Stability Indicating Assay for the Determination of Bilastine in Bulk Drug and Method Development Validation by RP-HPLC Using Analytical Quality by Design Approaches.” Indian Journal of Pharmaceutical Education & Research 58 (April): S582–90. doi:10.5530/ijper.58.2s.61.