<?xml version='1.0' encoding='utf-8'?>
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<records>
	
		
		 <record>
			<rec-number>108660</rec-number>
			<ref-type name="Report"></ref-type>
			<contributors>
				<authors>
					
						<author>Hertz, Sharon</author>
					
						<author>Avigan, Mark</author>
					
				</authors>
				
			</contributors>
			<titles>
				<title>Recommendation on a Regulatory Decision for Propoxyphene-containing Products</title> 
				
					  
				
		        	<secondary-title>FDA Center for Drug Evaluation and Research. Memorandum to the File NDA 10-997 Darvon (propoxyphene hydrochloride) Capsules
NDA 16-862 Darvon-N (propoxyphene napsylate and acetaminophen) Tablets NDA 17-122 Darvocet-N 50 and Darvocet-N 100 (propoxyphene napsylate and acetaminophen) Tablets</secondary-title>
				      
			</titles>
			

			
			
			<issue>2865911</issue>
			<dates>
				<year>2010</year>
				<pub-dates>
					<date>Nov 18, 2010</date>
				</pub-dates>
			</dates>
			<pub-location>Washington, DC</pub-location>
			<publisher>United States Department of Health and Human Services</publisher>
			
			
						
			
			
			
				<urls>
					
						<pdf-urls>
							<url>http://www.fda.gov/downloads/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/UCM234349.pdf</url>
						</pdf-urls>
					
								
				</urls>
						
			


		</record>




	
</records>
