Author(s): Priyanka M. Salve, Rajendra K. Surawase

Email(s): priyankasalve1126@gmail.com

DOI: 10.52711/0975-4377.2021.00044   

Address: Priyanka M. Salve*, Rajendra K. Surawase
Loknete Dr.J.D. Pawar College of Pharmacy, Manur, Tal-Kalwan, Dist-Nashik-423501.
*Corresponding Author

Published In:   Volume - 13,      Issue - 4,     Year - 2021


ABSTRACT:
Metoprolol succinate is a ß1 selective antagonist used an anti-arrhythmic, antiagina, antihypertensive. sustained release tablet of metoprolol succinate were formulated using polymers. The half-life of drug is relatively 4-6 hours. The formulation of metoprolol succinate tablet were produced by direct compression or wet granulation method. The formulations were evaluated for thickness, hardness, weight variation, friability and dissolution, drug content all the physical characteristics of the formulated tablets were within acceptable limits. The dissolution studies of Metoprolol succinate sustained release tablets reflects USP specification NMT 25%by 1 hours, 20-40%by 4 hours,40-60%by 8 hours and more than 80% by 20 hrs.


Cite this article:
Priyanka M. Salve, Rajendra K. Surawase. Formulation Development and In-vitro Evaluation of Sustained Release Tablets of Metoprolol Succinate. Research Journal of Pharmaceutical Dosage Forms and Technology. 2021; 13(4):269-5. doi: 10.52711/0975-4377.2021.00044

Cite(Electronic):
Priyanka M. Salve, Rajendra K. Surawase. Formulation Development and In-vitro Evaluation of Sustained Release Tablets of Metoprolol Succinate. Research Journal of Pharmaceutical Dosage Forms and Technology. 2021; 13(4):269-5. doi: 10.52711/0975-4377.2021.00044   Available on: https://rjpdft.com/AbstractView.aspx?PID=2021-13-4-1


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