PROCESS VALIDATION OF COATED LARIAGO TABLET

Industrial Process Validation of Tablet Dosage Form: a Review

The present article gives an introduction and general overview on process validation of pharmaceutical manufacturing process especially tablet manufacturing process. The principal objective of dosage form design is to achieve a predictable therapeutic response to a drug included in a formulation which is capable of large scale manufacture with reproducible product quality. Solid dosage forms in...

Development and Validation of Dissolution Test Method for Andrographolide from Film Coated Polyherbal Tablet Formulation

The objective of present study was to develop and validate a dissolution test for polyherbal hepatoprotective tablets containing andrographolide with bio-relevant media. Different dissolution conditions such as basket (type I)/paddle (type II) agitation, rotation speed, dissolution medium and volume were evaluated. The dissolution samples were analyzed and validated using a high-performance liq...

A Novel Compression-Coated Tablet Dosage Form

www.pharmtech.com new chemical entity often is first formulated as a free-flowing granulation for encapsulation within hard gelatin capsules. During the course of clinical development, the drugcontaining granulation usually is modified for compaction into a tablet product. The tablet product subsequently may be film coated for taste masking, identification, or other purposes. Tablets are the mo...

the development and validation of dissolution method for donepezil tablet

Modulation of Venlafaxine Hydrochloride Release from Press Coated Matrix Tablet

The aim of present study was to prepare novel modified release press coated tablets of venlafaxine hydrochloride. Hydroxypropylmethylcellulose K4M and hydroxypropylmethylcellulose K100M were used as release modifier in core and coat, respectively. A 3(2) full factorial design was adopted in the optimization study. The drug to polymer ratio in core and coat were chosen as independent variables. ...