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NOTICE OF POSTPONEMENTFexofenadine Hydrochloride and Fexofenadine Hydrochloride CapsulesApril 6, 2005 USP has postponed indefinitely the official dates of the Fexofenadine Hydrochloride and Fexofenadine Hydrochloride Capsules monographs, which were published in the First Supplement to USP 28–NF 23 on pages 3227 and 3228 respectively. These monographs were originally slated to become official on April 1, 2005. The postponements are to provide additional time to further evaluate some of the tests, procedures, and acceptance criteria provided in the proposed monographs. The Pharmaceutical Analysis 1 Expert Committee is presently reviewing comments received concerning these monographs. The USP intends to publish, if necessary, additional proposed revisions in a future issue of Pharmacopeial Forum for further public review and comment. USP proposes that these monograph revisions go forward to official text once the public comments have been considered. Should you have any questions, please contact Karen A. Russo, Ph.D., Associate Director Noncomplex Actives and Excipients and liaison to the Pharmaceutical Analysis 1 Expert Committee (301-816-8379 or ). What's New
![]() USP recalled USP 33-NF 28 on Jan. 8, 2010. A reissue product will be available in April 2010.
PF 36(2), March-April 2010: IRAs and Errata (03/01/10) February Revision Bulletins (02/26/10) Protamine Monographs: Notice of Intent to Revise (02/26/10) New Draft Pending Standard for the month of February (02/26/10) PF 36(2), March-April 2010: Highlights (02/22/10) Calculation Tool for the Performance Verification Test (PVT) of Dissolution Assemblies (02/22/10) Performance of Equipment to Test Dissolution of Medications Further Assured (02/09/10) New Official Text (01/29/10) Related Resources |
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