The present investigation is aimed at formulating and evaluating Extended release tablets of Venlafaxine Hcl using different polymers such as HPMC K4M, Eudragit RL-100.Venlafaxine Hydrochloride used for the management of major depressive disorder. Different concentrations of the polymers were taken. The physical mixture was evaluated prior to compression for determining the flow properties. These tablets were evaluated for weight variation, hardness, thickness, friability, content uniformity and in-vitro drug release profile. It was found that the formulation F3 containing HPMC K4M Polymer release 99% of drug In 24 hours time period and it is selected as a optimized formulation. Drug –Excipient interactions of pure drug and optimized formul...
Venlafaxine er serótónín-norepinefrín endurupptökuhemill sem er notaður sem þunglyndislyf. Markmið v...
This study is to check the selected polymer’s sustained drug delivery efficacy. The primary goal o...
 Objectives: The purpose of this study was to design a suitable transdermal therapeutic system for ...
Abstract- Venlafaxine Hcl is an anti-depressant drug which is used in depression. The aim of present...
Copyright © 2013 Shital Bhavin Butani. This is an open access article distributed under the Creative...
Venlafaxine hydrochloride, the salt form of venlafaxine, is a highly water soluble and atypical anti...
The aim of the present study was to develop a tablet formulation for sustained release of venlafaxin...
Objective: The present study was undertaken to prolong the release of orally administered drug. The ...
Objective: The sustained release of drug from the dosage form is useful especially for achieving con...
To select the suitable concentration level of controlled release polymer for the formulation of pred...
Objective : Venlafaxine,hydrochloride is a structurally novel phenethyl bicyclic antidepressant, and...
The present study was aimed to formulate and evaluate the Papaverine extended release tablet using p...
The aim of the current study was to design sustained release tablet of Diltiazem hydrochloride and t...
The present work is aimed at preparing and evaluating sustained release (SR) matrix tablets of valac...
AbstractThe present study was undertaken with an aim to formulate, develop and evaluate gastroretent...
Venlafaxine er serótónín-norepinefrín endurupptökuhemill sem er notaður sem þunglyndislyf. Markmið v...
This study is to check the selected polymer’s sustained drug delivery efficacy. The primary goal o...
 Objectives: The purpose of this study was to design a suitable transdermal therapeutic system for ...
Abstract- Venlafaxine Hcl is an anti-depressant drug which is used in depression. The aim of present...
Copyright © 2013 Shital Bhavin Butani. This is an open access article distributed under the Creative...
Venlafaxine hydrochloride, the salt form of venlafaxine, is a highly water soluble and atypical anti...
The aim of the present study was to develop a tablet formulation for sustained release of venlafaxin...
Objective: The present study was undertaken to prolong the release of orally administered drug. The ...
Objective: The sustained release of drug from the dosage form is useful especially for achieving con...
To select the suitable concentration level of controlled release polymer for the formulation of pred...
Objective : Venlafaxine,hydrochloride is a structurally novel phenethyl bicyclic antidepressant, and...
The present study was aimed to formulate and evaluate the Papaverine extended release tablet using p...
The aim of the current study was to design sustained release tablet of Diltiazem hydrochloride and t...
The present work is aimed at preparing and evaluating sustained release (SR) matrix tablets of valac...
AbstractThe present study was undertaken with an aim to formulate, develop and evaluate gastroretent...
Venlafaxine er serótónín-norepinefrín endurupptökuhemill sem er notaður sem þunglyndislyf. Markmið v...
This study is to check the selected polymer’s sustained drug delivery efficacy. The primary goal o...
 Objectives: The purpose of this study was to design a suitable transdermal therapeutic system for ...