Update: 1
From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Fri, 18 Apr 2008 06:08:58 -0500 (CDT)
Subject: CDRH New Update
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| FDA Home Page | CDRH Home Page | Search | A-Z Index |  | |
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 | Date: April 18, 2008 |
The following new items were added to the CDRH web pages on April 17, 2008. Previous CDRH New Items can be found on the CDRHNew Page.
 | Consumer Information on: Talent™ Abdominal Stent Graft System - P070027 |  |
Update: 2
From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Fri, 18 Apr 2008 12:50:49 -0500 (CDT)
Subject: CDER New 4/16 - 17/2008
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April 17, 2008
April 16, 2008
- CDER issues "Review of Therapeutic Equivalence Generic Bupropion XL 300 mg and Wellbutrin XL 300 mg"
- Drugs@FDA Downloadable Data Files (updated)
- Inactive Ingredient Search for Approved Drug Products
- New and Generic Drug Approvals
- Advicor (niacin lovastatin) Extended Release Tablets, Abbott Labs, Labeling Revision
- Diprivan (propofol) Injection, APP Pharma, Labeling Revision
- Nallpen in Plastic Container (nafcillin sodium) Injection, Baxter Healthcare, Labeling Revision
- Ofloxacin Ophthalmic Solution, Akorn Inc., Approval
- TriCor (fenofibrate) Tablets, Abbott Labs, Labeling Revision
Update: 3
From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Fri, 18 Apr 2008 15:06:00 -0500 (CDT)
Subject: California Department of Public Health Warns Consumers Not to Eat Chaca Chaca Chacatrozo Candy Imported from Mexico (April 17)
California Department of Public Health Warns Consumers Not to Eat Chaca Chaca Chacatrozo Candy Imported from Mexico (April 17)
Fri, 18 Apr 2008 14:51:00 -0500
Dr. Mark Horton, director of the California Department of Public Health (CDPH), today warned consumers not to eat Chaca Chaca Chacatrozo candy imported from Mexico after tests by CDPH found levels of lead that could cause health problems.
Update: 4
From: "U.S. Food & Drug Administration (FDA)" <fda@service.govdelivery.com>
Date: Fri, 18 Apr 2008 23:54:24 -0500 (CDT)
Subject: U.S. Food & Drug Administration (FDA) Genomics at FDA Update
Each year the US Food and Drug Administration expends considerable resources convening over 60 advisory committee meetings. This is part of our commitment to engage a wide range of scientific expertise to inform our regulatory decision making process. This is the right thing to do for we must keep up-to-date with the rapidly-changing world of science related to the products we regulate.
My take on this is that something so important deserves careful scrutiny to assure we are doing it the right way. Our Advisory Committee function is therefore one of my highest priorities in our Agency wide process-improvement effort.
The FDA this Week: http://www.fda.gov/oc/vonEschenbach/andys_take/default.html
Archive: http://www.fda.gov/oc/vonEschenbach/andys_take/archive_andys_take.html
This communications from the Commissioner for Food and Drugs, Andrew von Eschenbach, will discuss weekly FDA issues of interest to the American consumer and occasionally preview upcoming FDA issues and events.
This service is provided to you at no charge by U.S. Food & Drug Administration (FDA).
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