Formulation and development of tablets pdf

FORMULATION AND DEVELOPMENT OF FAST DISINTIGRATING TABLETS USING RANITIDINE HCL AS A MODEL DRUG ABSTRACT The present study was aimed towards the formulation and development of fast disintegrating tablets by ing Ranitidine HCl as a model drug. Fast disintegrating tablet of Ranitidine

unpleasant taste. Successful tablet formulation development involves the careful selection of ingredients in order to manufacture a robust solid dosage form. Choosing the appropriate excipient to perform a specific function in a tablet formulation such as disintegration or

The aim of the present project is formulation development, evaluation and comparative study of superdisintergrants in the Cefixime 50 mg oral disintegrating tablet. With the proof of different evaluation parameters listed in Table 8, it was concluded that C 3 (CCS) was the best formulation. In vitro dispersion time was measured by dropping a tablet in a beaker containing 100 mL of phosphate buffer (pH 6.8). Three tablets from each formulation were randomly selected and in vitro dispersion time was performed. Estimation of drug content Twenty tablets were powdered, and 100 mg equivalent weight of zidovudine tablet powder formulation the use or highly. The basic approach used in development of FDT was the use of superdi-sintegrants like cross linked Croscarmellose Sodium, Polyvinyl Pyrrolidone K30, Microcrystalline Cellulose, Crospovidone etc. which provide instan-taneous disintegration of tablet after placed on tongue, thereby releasing the drug in saliva.

Academia.edu is a platform for academics to share research papers. May 03, 2015 · Tablet Formulation Technology 1. Maksud Al- Hasan (Mahim) 2. Tablet is defined as a compressed solid dosage form containing medicaments with or without excipients. According to the Indian Pharmacopoeia Pharmaceutical tablets are solid, flat or biconvex dishes, unit dosage form, prepared by compressing a drug or a mixture of dru In vitro dispersion time was measured by dropping a tablet in a beaker containing 100 mL of phosphate buffer (pH 6.8). Three tablets from each formulation were randomly selected and in vitro dispersion time was performed. Estimation of drug content Twenty tablets were powdered, and 100 mg equivalent weight of zidovudine tablet powder Design, Development and Formulation of Orodispersible Tablets of a Model Drug Using Response Surface Methodology. Pharm Anal Acta 2012; 3:195 Abdul Althaf S, Sailaja PB, Ashwin Kumar M. Formulation, Evaluation and Mathematical Modelling of Clopidogrel Bisulphate & Aspirin Immediate Release Bilayer Tablets. formulation the use or highly. The basic approach used in development of FDT was the use of superdi-sintegrants like cross linked Croscarmellose Sodium, Polyvinyl Pyrrolidone K30, Microcrystalline Cellulose, Crospovidone etc. which provide instan-taneous disintegration of tablet after placed on tongue, thereby releasing the drug in saliva.