Abstract
Drugs as well as poor liquid efficiency and people enduring decadency in the aqueous medium might be in preference to formulated as solid products that include pills, powders, etc. The test that is carried out through the manufac- ture of impressive product comprises thickness, hardness, friability, dissolu- tion time, disintegration time. The objective consisting of the present report was to document the requirements for the manufacturing of semisolid com- pounds. Ointments and creams are semisolid compounds given that external application program to the skin. The present report deals with an elaborated overview of comparative study in-process along with the finished product QC test for parenteral preparation. Injectables stay at substantial prominence on the earth market regardless of growing within the pharmaceutical grocery for 2-3 years.
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CITATION STYLE
B","email":"prathapnila@gmail.com","affiliation":"Department, {"name":"Prathap, K","email":"prathapnila@gmail.com","affiliation":"Dhanalaksh, {"name":"Ananth, A","email":"prathapnila@gmail.com","affiliation":"Dhanalaksh, {"name":"Arthi, A","email":"prathapnila@gmail.com","affiliation":"Dhanalaksh, {"name":"Arunagiri, & R","email":"prathapnila@gmail.com","affiliation":"Dhanalaksh, {"name":"Balaji. (2021). Quality Control Test for Pharmaceutical Dosage Forms: A Review. Future Journal of Pharmaceuticals and Health Sciences, 1(4), 227–233. https://doi.org/10.26452/fjphs.v1i4.205
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