Development of a drug release methodology for carbamazepine CR tablets based on bioequivalence evaluation-Reference-Cited by-同舟云学术

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Development of a drug release methodology for carbamazepine CR tablets based on bioequivalence evaluation

Published:2008 Issue:2 Volume:18 Page:139-144
ISSN:1773-2247
Container-title:Journal of Drug Delivery Science and Technology
language:en
Short-container-title:Journal of Drug Delivery Science and Technology

Author:

Homšek I.,Parojčić J.,Mitić M.,Simić S.,Cvetković N.,Đurić Z.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference37 articles.

1. FDA requirements for controlled release products;Malinowski,1999

2. Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards;Lobenberg;Eur. J. Pharm. Biopharm.,2000

3. Martindale,The Extra Pharmacopoeia,2005

4. Controlled, multidose, pharmacokinetic evaluation of two extended-release carbamazepine formulations (Carbatrol and Tegretol-XR);Stevens;J. Pharm. Sci.,1998

5. Existing and new criteria for bioequivalence evaluation of new controlled release products of carbamazepine;Bialer;Epilepsy Res.,1998

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prolonged-release minitablets with carbamazepine – preliminary observations in vitro;Journal of Pharmacy and Pharmacology;2016-12-20

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