AVANIR Pharmaceuticals (FRA:AV2B) Short-Term Debt : €0.00 Mil (As of Sep. 2014)

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What is AVANIR Pharmaceuticals Short-Term Debt?

AVANIR Pharmaceuticals's Short-Term Debt for the quarter that ended in Sep. 2014 was €0.00 Mil.

AVANIR Pharmaceuticals's quarterly Short-Term Debt increased from Mar. 2014 (€8.07 Mil) to Jun. 2014 (€8.43 Mil) but then declined from Jun. 2014 (€8.43 Mil) to Sep. 2014 (€0.00 Mil).

AVANIR Pharmaceuticals's annual Short-Term Debt increased from Sep. 2012 (€1.68 Mil) to Sep. 2013 (€5.94 Mil) but then declined from Sep. 2013 (€5.94 Mil) to Sep. 2014 (€0.00 Mil).

AVANIR Pharmaceuticals Short-Term Debt Historical Data

The historical data trend for AVANIR Pharmaceuticals's Short-Term Debt can be seen below:

* For Operating Data section: All numbers are indicated by the unit behind each term and all currency related amount are in USD.
* For other sections: All numbers are in millions except for per share data, ratio, and percentage. All currency related amount are indicated in the company's associated stock exchange currency.

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AVANIR Pharmaceuticals Short-Term Debt Chart

AVANIR Pharmaceuticals Annual Data

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Sep14

Short-Term Debt

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1.68

5.94

AVANIR Pharmaceuticals Quarterly Data
	Dec09	Mar10	Jun10	Sep10	Dec10	Mar11	Jun11	Sep11	Dec11	Mar12	Jun12	Sep12	Dec12	Mar13	Jun13	Sep13	Dec13	Mar14	Jun14	Sep14
Short-Term Debt	Get a 7-Day Free Trial															5.94	7.94	8.07	8.43	-

AVANIR Pharmaceuticals Short-Term Debt Explanation

Short-Term Debt represents the total amount of Long-Term Debt such as bank loans and commercial paper, which is due within one year.

AVANIR Pharmaceuticals Short-Term Debt Related Terms

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AVANIR Pharmaceuticals (FRA:AV2B) Business Description

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Website

http://www.avanir.com

Avanir Pharmaceuticals was incorporated in California in August 1988 and was reincorporated in Delaware in March 2009. The Company is a biopharmaceutical company focused on acquiring, developing and commercializing novel therapeutic products for the treatment of central nervous system disorders. The Company commenced promotion of NUEDEXTA in the United States in February 2011. The Company is also studying AVP-923 for use in different types of neuropathic pain. NUEDEXTA is the first and only FDA-approved treatment for pseudobulbar affect. NUEDEXTA is an combination of two components: dextromethorphan hydrobromide, the ingredient that is harmacologically active in the central nervous system, and quinidine sulfate, a metabolic inhibitor enabling dextromethorphan to reach therapeutic plasma concentrations. The Company currently markets NUEDEXTA to approximately 10,000 physicians and other healthcare providers who specialize in psychiatry, neurology or geriatric medicine and practice in outpatient or long-term care settings. NUEDEXTA may face competition from several products: Antidepressants, including Prozac, Celexa, Zoloft, Paxil, Elavil and Pamelor and others; Atypical antipsychotic agents, including Zyprexa, Risperdal, Seroquel, Abilify, Geodon and others; and Miscellaneous agents, including Symmetrel, Lithium and others. The Company is subject to regulation under the Occupational Safety and Health Act, the Environmental Protection Act, the Toxic Substance Control Act, the Export Control Act and other present and future laws of general application.

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