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Apr 22, 2013
 |  BC Week In Review  |  Clinical News  |  Regulatory

Levadex dihydroergotamine regulatory update

Allergan said FDA issued a complete response letter for a resubmitted NDA for Levadex dihydroergotamine for the acute treatment of migraines in adults. The company said it has already addressed the main issues raised by FDA in the letter, including a facility inspection of a third-party manufacturer and...

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