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Journal :   Research Journal of Pharmacy and Technology

Volume No. :   6

Issue No. :  4

Year :  2013

Pages :   415-421

ISSN Print :  0974-3618

ISSN Online :  0974-360X


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Process Validation of Escitalopram oxalate 5 mg Tablet

Address:   Priyanka Upadhyay1, Rupesh Pandey2 and R.K. Pothal2
1Gayatri College of Pharmacy Rourkela Orissa
2Vivikanand College of Pharmacy, Indore (M.P.)
*Corresponding Author
DOI No: Not Available

Effective process validation contributes significantly to assuring drug quality. Process Validation of Escitalopram oxalate Tablet 5 mg strength was developed for the quality control and quality assurance purpose. In Vitro dissolution study was carried out using USP II apparatus (paddle apparatus). The crushing strength Kg/cm2 of prepared tablets was determined for 10 tablets of and standard deviation was determined for each batch. The average hardness and standard deviation was studied. Assay was performed to know the content of drug substance by UV spectrophotometer. The Method was validated in accordance to ICH guidelines.
Process Validation of Escitalopram oxalate 5 mg Tablet.
Priyanka Upadhyay, Rupesh Pandey, R.K. Pothal. Process Validation of Escitalopram oxalate 5 mg Tablet. Research J. Pharm. and Tech. 6(4): April 2013; Page 422-427.
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