Stability Indicating RP-HPLC Method Development and Validation for the Determination of Solifenacin Succinate in Bulk and its Pharmaceutical Formulation
Author:
Affiliation:
1. Department of Pharmaceutical Analysis and Quality Assurance, GIP, GITAM (Deemed to be University), Rushikonda, Visakhapatnam - 530045, India.
2. Scientist, FRD, Dr. Reddy’s Laboratories, IPDO, Bachupally, Hyderabad - 500090, India.
Abstract
Publisher
A and V Publications
Subject
Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Reference20 articles.
1. Bhavana V, Kumar HT, Rao SY, Rao VP. RP-HPLC Method for Estimation of Solifenacin Succinate in API and Tablet Dosage Form. Asian Journal of Pharmaceutical Analysis. 2019; 9(3): 118-22.
2. Chandra Mohan T, Hemalatha B, Shainy B, Vasundhara G, Sandhya S, Ashok Kumar A. A rapid RP-HPLC method development and validation for the quantitative estimation of solifenacin succinate in tablets. International Journal of Pharmacy and Pharmaceutical Sciences. 2014; 6: 201-4.
3. Ganthi HK, Reddy R, Park YJ, Bapatu HR, Park SJ, Cho WH. Stability indicating HPLC method for quantification of solifenacin succinate & tamsulosin hydrochloride along with its impurities in tablet dosage form. American Journal of Analytical Chemistry. 2016; 7(11): 840-62.
4. Reddy R, Sidhaye R, Sherikar AV, Nadre M, Krishna M. Development and Validation of A Stability Indicating Analytical Method For Determination of Related Substances by RPHPLC For Solifenacin Succinate in Solifenacin Succinate Tablets. Pharmacophore. 2017; 8(2): 142-149.
5. Rakesh B, Bhargavi P, Reddy SR, Kumar AA. UV-Spectrophotometric method development and validation for the quantitative estimation of solifenacin succinate in tablets. Int J Pharm Pharm Sci. 2014; 6:190-3.
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