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Teva files albuterol multi- dose dry powder inhaler at FDA to treat Bronchospasm.

Read time: 1 mins
Last updated:15th Jul 2014
Published:15th Jul 2014
Source: Pharmawand

Teva Pharmaceuticals Industries Ltd., announced that the FDA has accepted for review the company�s new drug application (NDA) for albuterol multi-dose dry-powder inhaler (MDPI), an investigational breath-actuated dry-powder inhaler for the treatment or prevention of Bronchospasm in patients 12 years of age and older with reversible obstructive airway disease; and for the prevention of exercise-induced Bronchospasm (EIB) in patients 12 years of age and older.

A response by the US Food and Drug Administration is expected in March 2015.

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