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RP-HPLC method development and validation of carvedilol in bulk and pharmaceutical dosage forms |
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| | Koteswari, P., Ramakrishna, S., Reddy, V.P., Janani, V.R., Sireesha, K.R., Narasu, L.M. | | | Journal of Chemical and Pharmaceutical Sciences. 2011; 4(1): 19-21 | | | [Pubmed] [Google Scholar] | | | 2 |
Preparation and evaluation of self-microemulsifying drug delivery system of carvedilol |
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| | Rao, M.R.P., Munjapara, G.S., Khole, I.A. | | | Latin American Journal of Pharmacy. 2011; 30(5): 837-843 | | | [Pubmed] [Google Scholar] | | | 3 |
Ezetimibe (book) |
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| | Lestari, M.L.A.D., Ardiana, F., Indrayanto, G. | | | Profiles of Drug Substances, Excipients and Related Methodology. 2011; 36: 103-149 | | | [Pubmed] [Google Scholar] | | | 4 |
Quantitative determination and validation of Carvedilol in pharmaceuticals using quantitative nuclear magnetic resonance spectroscopy |
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| | Hemant Gadape, Kalpesh Parikh | | | Analytical Methods. 2011; 3(10): 2341 | | | [HTML Full text] [Google Scholar] | | | 5 |
Development of carvedilol assay in tablet dosage form using HPLC with fluorescence detection |
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| | Sripalakit, P., Kaewnok, S., Tubtonglang, S. | | | Maejo International Journal of Science and Technology. 2010; 4(1): 8-19 | | | [Pubmed] [Google Scholar] | |
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