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Pharmaceutical Development and Technology Volume 6, 2001 - Issue 1
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Research Article

A Better Dissolution Method for Ranitidine Tablets USP

Michael L. Cappola
Pages 11-17 | Received 30 Jan 2000, Accepted 27 Mar 2000, Published online: 25 Jan 2001

Citations (5)

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Yan Wu, D. O. Kildsig & E. S. Ghaly. (2004) Effect of Hydrodynamic Environment on Tablets Dissolution Rate. Pharmaceutical Development and Technology 9:1, pages 25-37.
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Articles from other publishers (4)

P. Zarmpi, T. Flanagan, E. Meehan, J. Mann, J. Østergaard & N. Fotaki. (2020) Biopharmaceutical implications of excipient variability on drug dissolution from immediate release products. European Journal of Pharmaceutics and Biopharmaceutics 154, pages 195-209.
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Shayne Cox GadA.K. Tiwary, Bharti Sapra & Subheet Jain. 2010. Pharmaceutical Sciences Encyclopedia. Pharmaceutical Sciences Encyclopedia.
Francisco J. Flores‐Murrieta, Alejandra Toledo, Miriam del Carmen Carrasco‐Portugal, Gerardo Reyes‐García, Juan Rodríguez‐Silverio, Roberto Medina‐Santillán & Jorge E. Herrera. (2005) Comparative bioavailability of two oral formulations of ranitidine. Biopharmaceutics & Drug Disposition 27:1, pages 23-27.
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H. Kortejärvi, M. Yliperttula, J.B. Dressman, H.E. Junginger, K.K. Midha, V.P. Shah & D.M. Barends. (2005) Biowaiver monographs for immediate release solid oral dosage forms: Ranitidine hydrochloride. Journal of Pharmaceutical Sciences 94:8, pages 1617-1625.
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