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Process Validation Of Cefpodoxime Proxetil Oral Suspension I.P.

Show simple item record Joshi, Priya 2020-11-10T06:36:27Z 2020-11-10T06:36:27Z 2011-06-06
dc.description For Full Thesis Kindly contact to respective Library en_US
dc.description.abstract The aim of this work was to study process validation of cefpodoxime proxetil oral suspension I.P. Three initial process validation batches of same size, method, equipment and validation criteria were taken. The critical parameters involved in sifting, mixing, drying and filling were identified and evaluated as per validation master plan. All the instruments were calibrated as per standard operating procedures. Uniformity of blending was optimum in 60 minutes as standard deviation is between ±0.31 to ±0.37. Drying time of 60 min was suitable for obtaining moisture content within 0.3-.06%. The Drug content of reconstituted liquid suspension on day 1 and at day 7 were within the limits of 90% to 110%. The outcome indicated that data obtained by process validation of three batches provides high degree of assurance that manufacturing process of cefpodoxime proxetil oral suspension produces product meeting its predetermined specifications and quality attributes. en_US
dc.language.iso en en_US
dc.publisher Parul University en_US
dc.subject 092140804009 en_US
dc.title Process Validation Of Cefpodoxime Proxetil Oral Suspension I.P. en_US
dc.title.alternative 092140804009 en_US
dc.type Thesis en_US

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