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Tag Archives: Tablets

Simultaneous Estimation of Moxonidine and Hydrochlorothiazide in Tablets by RP-HPLC

A. Thenmozhi, H. Mubeena*, N. Venkateshan Department of Pharmaceutical Analysis, Arulmigu Kalasalingam College of Pharmacy, Anand Nagar, Krishnankoil -626 190, Tamil Nadu. A  B  S  T  R  A  C  T A simple, precise, specific sensitive and accurate reverse phase high performance liquid chromatographic (HPLC) method was developed for the determination of Moxonidine and Hydrochlorothiazide in tablet dosage form. The separation ... Read More »

Fabrication of Lansoprazole sustained Release Matrix Tablets: In vitro evaluation

Vani N, Hindustan Abdul Ahad, Prathima G, Manuja T, Amani P Balaji College of Pharmacy, Ananthapuramu, Andhra Pradesh, India A B S T R A C T The main objective of the present study was to develop matrix tablets of Lansoprazole and to study its sustained release for prolonged time in tablet formulations. Compatibility of Lansoprazole with excipients used was ... Read More »

Development and Validation of RP-HPLC Method for the Estimation of Sitagliptin Phosphate in Bulk and Its Tablet Dosage Form

I. Arulraj1, P. Vembu2 and A. Chenthilnathan1* 1Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli – 627 012, Tamil Nadu, India. 2Bafna Pharmaceuticals Limited, Grantlyon village, Chennai – 600 052, Tamil Nadu, India. A B S T R A C T A simple and sensitive reversed-phase liquid chromatographic method has been developed and validated for the estimation of Sitagliptin phosphate ... Read More »

Design and Characterization of Controlled Release Tablets of Emtricitabine by Compression Coating Technology

A. Prameela Rani, Varanasi. S. N. Murthy* University College of Pharmaceutical Sciences, Acharya Nagarjuna University, Guntur, Andhra Pradesh, India A B S T R A C T Extending or controlling the release of highly water soluble drugs from matrix tablets is always a challenge. The research attempt was aimed to explore the compression coating technology for the development of controlled ... Read More »

Analytical Method Development and Validation by RP-HPLC for the Simultaneous Estimation of Linagliptin and Metformin in Bulk and Combined Tablet Dosage Form

G. Varun Kumar*, V. Pavan kumar, M. Gobinath, V. Hari Baskar, Ramesh Dhani, Y. Vijitha Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Muthukur, SPSR Nellore, A.P, India A B S T R A C T A new simple accurate and suitable reverse phase high performance liquid chromatographic method was developed for the determination of Metformin and Linagliptin in ... Read More »

Method Development and Validation of Ondansetron in Bulk and Pharmaceutical Dosage Form by UV Spectrophotometer

P. Leena sruthi*, C. Ravindra Reddy, V. Sagarika, K. Girish, V. G. P. Sivakumar                          Department of Pharmaceutical Analysis, Balaji College of Pharmacy, Anantapur–515001, AP, India A B S T R A C T A simple, rapid, precise, accurate and sensitive analytical method was developed for the UV spectrophotometric ... Read More »

Improved Tablet Production by Modified Granulation Techniques – A Review

B. Venkateswara Reddy*, K. Navaneetha, P. Sandeep, P. Ujwala Department of Pharmaceutics, St.Pauls College of Pharmacy, Turkayamjal , Hayathnagar , Ranga Reddy -501510 Abstract Tablets are one of the oral solid dosage forms most widely used by the pharmaceutical manufacturers, physicians and patients due to the convenience in manufacturing, administration and suitability for delivery of most of the active ingredients. ... Read More »

Formulation and Evaluation of Immediate Release Donepezil Tablets

Taj khan H*, Hindustan Abdul Ahad, Naresh G, Sreekanth K  PG Department of Pharmaceutics, Balaji college of pharmacy, Ananthapuramu-515 001, Andhra Pradesh, India Abstract The study was undertaken with an aim to develop an optimized formulation of anti-Alzheimer, Donepezil HCl by oral drug delivery. Preformulation studies were conducted to know the drug excipients compatibilities. Based on the results, suitable excipients ... Read More »

Formulation and Evaluation of Abacavir Sulphate Sustained Release Tablets

Anand Babu U*, Hindustan Abdul Ahad, Sreedhar V, Bala Chandu M PG Department of pharmaceutics, Balaji College of pharmacy, Ananthapuramu, Andhra Pradesh, India APOTHEKE-2014, 8 Nov 2014, Organized by Balaji College of Pharmacy, Ananthapuramu, Andhra Pradesh, India Abstract The main objective of the present study was to formulate once a daily dose of Abacavir Sulphate sustained release tablets by direct ... Read More »

Design and Novel Approaches of Orally Disintegrating Tablets

Author Details S.S Siddheshwar*1, R.K. Godge 2, M.H.Kolhe1, S.D.Mankar1 1Department of Pharmaceutics, P.R.E.S.’s, Pravara Rural College of Pharmacy, Loni, India 2Department of Pharmaceutical Chemistry, P.R.E.S.’s, Pravara Rural College of Pharmacy, Loni, India Abstract Tablets designed to dissolve on the buccal (cheek) mucous membrane were a precursor to the ODT. This dosage form was intended for drugs that yield low bioavailability through the digestive tract ... Read More »

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