A-Z Index
Image Cart
              

 Information For:

Manufacturers

Regulator

Healthcare

Consumers

Members


Revision Bulletin

Ethinyl Estradiol Tablets Monograph

Posting Date: May 29, 2009
Official Date: July 1, 2009
Expert Committee: Biopharmaceutics
Transfers to Accelerated Revision History: 1 May 2010


In accordance with the Rules and Procedures of the 2005-2010 Council of Experts, the Biopharmaceutics Expert Committee has revised the Ethinyl Estradiol Tablets Monograph by adding two Dissolution tests.

The Ethinyl Estradiol Tablets Revision Bulletin supersedes the Monograph in USP 32–NF 27 until it is printed in the USP 33–NF 28, which will be released 1 November 2009 and becomes official 1 May 2010.

Should you have any questions, please contact Margareth Marques, Ph.D. (301–816–8106 or .

Download the Ethinyl Estradiol Tablets Monograph  (105KB)

What's New

Changes to the Dissolution Performance Verification Test (11/20/09)

PF 35(6) Errata (10/30/09)

New official Text for October: 15 Revisions Bulletins (10/30/09)

Pending Standards for the month of October (10/30/09)

PF 35(6), November-December 2009: Highlights and Stimuli Articles (10/23/09)

Admission Criteria and Safety Classification for Dietary Supplements Guideline (10/22/09)

Elemental Impurities Hot Topics information updated (10/13/09)

General Chapter <1151> Pharmaceutical Dosage Forms (10/06/09)

Heparin Hot Topics information updated (10/02/09)

PF Redesign

Related Resources