Author(s): Packiaraj Jeyachandran Manohari, Venkateswaran Chidambaram Seshadri, Narendra Reddy Parvatha Janarthana Reddy, Sumathi Vinay Rao, Harshavardhana Reddy Venkatarangareddy, Janakiraman Kunchithapatham, Mahendhirababu Sankar, Guhan Himadeep Chowdary Eswara Rao, Srihariteja Seelamantula, Sathyanarayana Reddy Sanivarapu Venkata

Email(s): Packiaraj.jm@hibrowhealthcare.com

DOI: 10.52711/0974-360X.2022.00699   

Address: Packiaraj Jeyachandran Manohari1*, Venkateswaran Chidambaram Seshadri1, Narendra Reddy Parvatha Janarthana Reddy1, Sumathi Vinay Rao1, Harshavardhana Reddy Venkatarangareddy1, Janakiraman Kunchithapatham2, Mahendhirababu Sankar1, Guhan Himadeep Chowdary Eswara Rao1, Srihariteja Seelamantula1, Sathyanarayana Reddy Sanivarapu Venkata1
1Hibrow Healthcare Pvt Ltd and Nutrimed Lifesciences Pvt Ltd, Survey No. 258, Thiruvandavar Village, Sirupinayur Taluk, Uthiramerur Panchayat, Kanchipuram District, Via Mamandoor - Uthiramerur Road, Chengalpet – 603308, Chennai, Tamil Nadu, India.
2Professor and Head of the Department, Department of Pharmacy, Annamalai University, Annamalai Nagar - 608002, Tamil Nadu, India.
*Corresponding Author

Published In:   Volume - 15,      Issue - 9,     Year - 2022


ABSTRACT:
In this research an attempt was made to develop and evaluate a commercially feasible and cost-effective tablet and oral suspension of Solifenacin Succinate. In international market, Solifenacin Succinate is available in both tablet and oral suspension dosage form. In Indian market, only tablet dosage form is available. Hence it was decided to make a formulation of Solifenacin Succinate that will not only be used as an oral solid dosage form in the form of tablet but also can be readily converted to oral suspension by extemporaneous means. A simple direct blending process was followed using limited excipients to make the end product cost-effective. The finalized product was comparable to the international brand product with respect to physico-chemical attributes, drug release and stability. The prepared tablet was made into an oral suspension using Ora-Plus® and Ora-Sweet® and the compounded suspension showed good palatability, organoleptics, chemical and microbial stability.


Cite this article:
Packiaraj Jeyachandran Manohari, Venkateswaran Chidambaram Seshadri, Narendra Reddy Parvatha Janarthana Reddy, Sumathi Vinay Rao, Harshavardhana Reddy Venkatarangareddy, Janakiraman Kunchithapatham, Mahendhirababu Sankar, Guhan Himadeep Chowdary Eswara Rao, Srihariteja Seelamantula, Sathyanarayana Reddy Sanivarapu Venkata. Development of commercially feasible and Cost-effective tablet of Solifenacin succinate that can be compounded into an oral suspension. Research Journal of Pharmacy and Technology. 2022; 15(9):4166-2. doi: 10.52711/0974-360X.2022.00699

Cite(Electronic):
Packiaraj Jeyachandran Manohari, Venkateswaran Chidambaram Seshadri, Narendra Reddy Parvatha Janarthana Reddy, Sumathi Vinay Rao, Harshavardhana Reddy Venkatarangareddy, Janakiraman Kunchithapatham, Mahendhirababu Sankar, Guhan Himadeep Chowdary Eswara Rao, Srihariteja Seelamantula, Sathyanarayana Reddy Sanivarapu Venkata. Development of commercially feasible and Cost-effective tablet of Solifenacin succinate that can be compounded into an oral suspension. Research Journal of Pharmacy and Technology. 2022; 15(9):4166-2. doi: 10.52711/0974-360X.2022.00699   Available on: https://rjptonline.org/AbstractView.aspx?PID=2022-15-9-59


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