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FORMULATION AND EVALUATION OF CETIRIZINE DIHYDROCHLORIDE ORODISPERSIBLE TABLET
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| dc.contributor.author | SUBRAMANIAN, S | |
| dc.contributor.author | SANKAR, V | |
| dc.contributor.author | MANAKADAN, ASHA ASOKAN | |
| dc.contributor.author | ISMAIL, SAREENA | |
| dc.contributor.author | ANDHUVAN, G | |
| dc.date.accessioned | 2022-11-29T06:45:28Z | |
| dc.date.available | 2022-11-29T06:45:28Z | |
| dc.date.issued | 2010-04-19 | |
| dc.identifier.citation | Subramanian, S., Sankar, V., Manakadan, A. A., Ismail, S., & Andhuvan, G. (2010). Formulation and evaluation of Cetirizine dihydrochloride orodispersible tablet. Pakistan journal of pharmaceutical sciences, 23(2), 232-236. | en_US |
| dc.identifier.issn | 1011-601X | |
| dc.identifier.uri | http://142.54.178.187:9060/xmlui/handle/123456789/14219 | |
| dc.description.abstract | Cetirizine orodispersible tablets were prepared to achieve quick onset of action and for maximum bioavailability. Tablets were prepared using cetirizine along with camphor and mannitol in the proportion of 1:1:1, 1:1:3, and 1:1:6. The flow property of granules was found to be good for the formulation CZ2 (1:1:3). The hardness and friability of all the formulations were found to be within the standard limit for orodispersible tablets. Disintegration time was found to be rapid in formulation CZ2 (1:1:3).The in vitro dissolution time was found to be 100% in 11 minutes for the formulation CZ2 (1:1:3). | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Karachi: Faculty of Pharmacy & Pharmaceutical Sciences, Karachi | en_US |
| dc.subject | Cetirizine orodispersible tablets | en_US |
| dc.subject | HPLC method | en_US |
| dc.subject | hausner ratio | en_US |
| dc.subject | wetting time | en_US |
| dc.title | FORMULATION AND EVALUATION OF CETIRIZINE DIHYDROCHLORIDE ORODISPERSIBLE TABLET | en_US |
| dc.type | Article | en_US |
