Citas bibligráficas
Carrera, N., (2021). Control de procesos en tabletas de diclofenaco sódico 50 mg + paracetamol 500 mg de un laboratorio farmacéutico nacional [Universidad Nacional de Trujillo]. https://hdl.handle.net/20.500.14414/19335
Carrera, N., Control de procesos en tabletas de diclofenaco sódico 50 mg + paracetamol 500 mg de un laboratorio farmacéutico nacional []. PE: Universidad Nacional de Trujillo; 2021. https://hdl.handle.net/20.500.14414/19335
@misc{renati/1048723,
title = "Control de procesos en tabletas de diclofenaco sódico 50 mg + paracetamol 500 mg de un laboratorio farmacéutico nacional",
author = "Carrera Alva, Noris Malú",
publisher = "Universidad Nacional de Trujillo",
year = "2021"
}
ABSTRACT The purpose of this pre-professional practice report was to describe the process control in diclofenac sodium 50 mg + paracetamol 500 mg tablets from a national pharmaceutical laboratory. Three batches of the product were evaluated to verify if the manufacturing process is reproducible. The methodology consisted of controlling the processes in the different stages: granulation, tableting, coating, finished product. The weight, hardness, friability, dimensions, disintegration and tightness tests were carried out. Likewise, the aspect of the primary and secondary packaging was verified, the number of units in each of them. The tests were based on the technical specifications for laboratory process control, having as reference the United States Pharmacopeia (USP 42 ). In conclusion, the three batches analyzed comply with the technical specifications established according to the national pharmaceutical laboratory's own standard with reference to the USP for each of the manufacturing stages.
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