the NDA for moxduoIR is to be refiled with the FDA with an expected decision in mid 2013.
previous presentations indicate that actavis was 'gearing up' in anticipation of earlier approval by employing additional sales staff etc. clearly that will have to be rewound. it appears atcavis will bear the cost of the delay at first instance. will those costs be borne by qrx when its entitlement to royalties are caculated?can anyone explain the basis on which royalties to qrx are calculated?
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