Wednesday , 19 June 2024

Tag Archives: Method development

Analytical Method Development and Validation for Apixaban by RP-HPLC

Md. Abdul Majeed*1, Dr.K.Vijaya1, B. Anitha2 1Department of Pharmaceutical Analysis, Monad Univeristys, Hapur, Rajasthan, India 2SARC (Scientific and Applied Research Center), Hyderabad, Telangana, India A B S T R A C T A simple and precise RP-HPLC method was developed for the determination of Apixaban dosage form the chromatographic separation was achieved on an Zorbax Bonus RP (250 X 4.6mm) ... Read More »

A Novel validated RP-HPLC method for the estimation of “Rupatadine” in its Bulk and Pharmaceutical Dosage forms

CH. Naveen Kumar*, Arvapalli Rajani, Vemula Madhavi Latha, Vijaya Kuchana Department of Pharmaceutical Analysis and Quality Assurance, Teegala Krishna Reddy College of Pharmacy, Hyderabad, India Abstract A Novel Reverse Phase High Performance Liquid Chromatography (RP-HPLC) method for the Estimation of “Rupatadine” has been developed. The developed method was found and proved to be a better one than the already existing ... Read More »

Estimation of Rabeprazole Sodium in tablet dosage form by using UV-VIS Spectrophotometer

About author Vipin Kumar Agrawal *, Alok Singh , Pravesh Kumar, Jyoti Rai, Inamullah Department of Pharmaceutics, Invertis Institute of Pharmacy, Invertis University, Bareilly-243 123, Uttar Pradesh, India Department of Pharmaceutical Chemistry, Invertis Institute of Pharmacy, Invertis University, Bareilly-243 123, Uttar Pradesh, India *E-mail: [email protected] Abstract Rabeprazole sodium (RSM) is a proton pump inhibitor used against peptic ulcer disease to ... Read More »

METHOD DEVELOPMENT AND VALIDATION OF EFAVIRENZ IN BULK AND PHARMACEUTICAL TABLET DOSAGE FORM BY USING UV–VISIBLE SPECTROPHOMETRIC METHOD

ABOUT AUTHOR Somsubhra Ghosh*, B. Rajni,  S. Vidyadhar, Dr. David Banji Department of Pharmaceutical Analysis and Quality Assurance, Nalanda College of pharmacy, Cherlapally, Nalgonda, Andhra Pradesh, India. E-mail : [email protected] ABSTRACT The present research work discusses the development of UV Spectrophotometric method for the determination of Efavirenz  in bulk and pharmaceutical capsule dosage form. The present method is simple, rapid, ... Read More »

Method development and validation for the simultaneous estimation of Nebivolol hydrochloride and S (-) Amlodipine besilate in tablet dosage form by RP – HPLC

About author Prabhakaran. V.*, Sekar. S., Baskar.E., Raghuprasath. V.R. Formulation Research and Development Department, The Madras Pharmaceuticals, Karapakkam, Chennai, Tamil Nadu, India. Email: [email protected] ABSTRACT High Performance Liquid Chromatography method was developed and validated in a simple, specific and precise manner for Nebivolol HCl and Amlodipine besilate in a combined solid dosage form. Nebivolol hydrochloride, a long acting, cardioselective β ... Read More »

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