Author(s): Priyanka Kailas Borse, Kiran B. Dhamak

Email(s): priyankaborse503@gmail.com

DOI: 10.52711/2231-5713.2021.00017   

Address: Priyanka Kailas Borse*, Kiran B. Dhamak
Department of Quality Assurance Techniques, PRES’s College of Pharmacy (For Women), Chincholi, Nashik, MS, India.
*Corresponding Author

Published In:   Volume - 11,      Issue - 2,     Year - 2021


ABSTRACT:
The plethora subscribed in this research is directed towards the process validation of tablet formulation containing Isoniazide and Rifampin. The different process parameters were identified and studied for the tablet formulation batches. Three process validation batches of same size, manufacturing process, equipment and validation criteria was taken. The critical parameter involved in sifting, dry mixing, preparation of granulating agent, wet mixing, wet milling, drying, sizing, lubrication and compression stages were identified and evaluated. The outcome indicated that this process validation data provides high degree of assurance that manufacturing process produces product meeting its predetermined specifications and quality attributes.


Cite this article:
Priyanka Kailas Borse, Kiran B. Dhamak. Process Validation of Isoniazide and Rifampin Tablet. Asian Journal of Pharmacy and Technology. 2021; 11(2):105-0. doi: 10.52711/2231-5713.2021.00017

Cite(Electronic):
Priyanka Kailas Borse, Kiran B. Dhamak. Process Validation of Isoniazide and Rifampin Tablet. Asian Journal of Pharmacy and Technology. 2021; 11(2):105-0. doi: 10.52711/2231-5713.2021.00017   Available on: https://ajptonline.com/AbstractView.aspx?PID=2021-11-2-2


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DOI: 10.5958/2231–5713 


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