In present study, the fast dissolving tablets of Amoxicillin Trihydrate were prepared by direct compression technique using microcrystalline cellulose (MCC) as direct compressible diluents. Sodium starch glycolate (SSG) and croscarmillose sodium (CCS) used as synthetic superdisintegrants. The swelling indices of the superdisintegrants were also compared. Among both the superdisintegrants, croscarmillose sodium showed the highest swelling index. The blends showed satisfactory flow properties. Eight formulations were prepared using different concentrations of Superdisintegrants and were investigated for their effect on the disintegration time and dissolution rate of the tablets. Tablets were also evaluated for weight variation, hardness, thic...
The demand of solid oral drug delivery systems has been growing during the last decade especially fo...
The present study was to formulation and optimization of fast dissolving tablet of terbutaline sulph...
An ideal drug therapy was based on relating pharmacological response to the dose administered. Poor ...
Objective: The present work is aimed to formulate fast dissolving stable tablet formulation a prefer...
An attempt was made to prepare fast dissolving tablets of anti-inflammatory drug Nimesulide preparin...
The aim of the present work is to formulate fast dispersible tablets of lactic acid bacillus & Z...
Amlodipine besylate is a recognized drug for hypertension therefore development of an ODT of Amlodip...
Omeprazole fast disintegrating tablets were prepared by using different superdisintegrants like cros...
The aim of this work is to prepare fast dissolving tablets of Diltiazem Hydrochloride to improve pat...
ABSTRACT:In the present study, novel co-processed superdisintegrants were developed by solvent evapo...
The amoxicillin 500 mg formulations were developed by direct compression using a 23 factorial design...
The Study was undertaken with an aim to formulate oro-dispersible tablets of cefuroxime axetil by us...
The aim of the present investigation was to develop fast dissolving tablets of Simvastatin, an lipid...
Fast dissolving tablets (FDT) of Granisetron hydrochloride were prepared by direct compression metho...
Fast disintegrating drug delivery system offers a solution for these patients having difficulty in s...
The demand of solid oral drug delivery systems has been growing during the last decade especially fo...
The present study was to formulation and optimization of fast dissolving tablet of terbutaline sulph...
An ideal drug therapy was based on relating pharmacological response to the dose administered. Poor ...
Objective: The present work is aimed to formulate fast dissolving stable tablet formulation a prefer...
An attempt was made to prepare fast dissolving tablets of anti-inflammatory drug Nimesulide preparin...
The aim of the present work is to formulate fast dispersible tablets of lactic acid bacillus & Z...
Amlodipine besylate is a recognized drug for hypertension therefore development of an ODT of Amlodip...
Omeprazole fast disintegrating tablets were prepared by using different superdisintegrants like cros...
The aim of this work is to prepare fast dissolving tablets of Diltiazem Hydrochloride to improve pat...
ABSTRACT:In the present study, novel co-processed superdisintegrants were developed by solvent evapo...
The amoxicillin 500 mg formulations were developed by direct compression using a 23 factorial design...
The Study was undertaken with an aim to formulate oro-dispersible tablets of cefuroxime axetil by us...
The aim of the present investigation was to develop fast dissolving tablets of Simvastatin, an lipid...
Fast dissolving tablets (FDT) of Granisetron hydrochloride were prepared by direct compression metho...
Fast disintegrating drug delivery system offers a solution for these patients having difficulty in s...
The demand of solid oral drug delivery systems has been growing during the last decade especially fo...
The present study was to formulation and optimization of fast dissolving tablet of terbutaline sulph...
An ideal drug therapy was based on relating pharmacological response to the dose administered. Poor ...