Development of Fast Disintegration Tablets As Oral Drug Deliverysystem :A Review

In view of the application of galactomannans in the develo- pment of solid pharmaceutical dosage forms in conventional or modiied drug delivery systems, particularly tablets

Using the drug β -CD complex, oro-dispersible tablets were prepared and evaluated for hardness, friability, weight variation, thickness, disintegrating time (DT), dissolution

Taste masked orally disintegrating oloxacin tablets were formulated for more palatable and compliance disin- tegration in oral cavity using Tulsion 335 and Indion 204

All the tablets of metoprolol tartrate were subjected to tests for weight variation, hardness, friability, in vitro dispersion, drug polymer interaction, drug content

ranitidine tablets of a reference drug (product A) and a generic (product B) and a similar (product C) drug marketed in Bahia, Brazil using a simple, fast and inexpensive

The directly compressed tablets from formulation F-1 to F-3 were evaluated for parameters viz., weight variation, hardness, friability, disintegration time, drug content, in-vitro

Granisetron Hydrochloride tablets were evaluated for post compression parameters like hardness, weight variation, thickness, friability, disintegration time, drug content and

Powder, granules and tablets were evaluated for several parameters, including flow properties, Carr and Hausner indexes, hardness, friability, disintegration time and drug