|
Information For:
|
Galantamine Tablets: Notice of Intent to Revise (Reposted)
In accordance with the Rules and Procedures of the Council of Experts, the Biopharmaceutics Expert Committee intends to revise the Galantamine Tablets monograph by adding another Dissolution test with a concomitant labeling requirement. The revisions to the Monograph will be made official in the near future as a Proposed Interim Revision Announcement. In the absence of any adverse comments, the revision will be published as final in Pharmacopeial Forum. The initial Notice of Intent to Revise for the Galantamine Tablets Monograph originally included revisions to impurities limits by the Monograph Development–Psychiatrics and Psychoactives Expert Committee. These changes were approved and published as an Interim Revision Announcement in PF 35(2) [Mar.–Apr. 2009]. See the original posting for Galantamine Tablets (posted 01–Aug–2008) in the Retired Compendial Notices section for more information. Should you have any questions please contact Margareth Marques, Ph.D., (301–816–8106 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 |
||||||||||||||||||||||||||||
Copyright © 2010 The United States Pharmacopeial Convention
|
|||||||||||||||||||||||||||||