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Rajkiran Kolakota*, Y. Rupavathi Department of Pharmaceutical Analysis, Sri Sivani College of Pharmacy, NH-16, Chilakapalem Jn, Srikakulam-532402, A.P ABSTRACT A HPLC method was developed and validated to determine trace amounts of levofloxacin related substances & degradation products in its formulation. Separation of levofloxacin from impurity A, impurity B, impurity C and unknown degradation products was achieved on a YMC-Pack Pro ... Read More »
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Analytical Method development for the Estimation of Related Substances by High performance Liquid Chromatographyfor the Rimonabent (RIM) drug
Dr. K. Mukkanti1, Dr. Srinivas Jagarlapudi2, Panchumarthi Srinivas*1, A. Ravi Kumar2, P. Ramyasree2 1Research Supervisor of Centre for Environment Institute of Science and Technology (Autonomous) Jawaharlal Nehru Technological University, Hyderabad, Telangana. India-500085. 2Obvez Labs Pvt. Ltd. Plot No. 22 & 23, ALEAP Industrial Area, Pragathi Nagar, Hyderabad, Telangana. India- 500090. A B S T R A C T The main aim ... Read More »
