FDA
approval
· 2011-12-27
FDA Approved: PAROXETINE — Supplemental Application (Mylan Pharmaceuticals Inc.)
Summary
FDA approved a supplemental application from Mylan Pharmaceuticals for paroxetine hydrochloride hemihydrate, authorizing a generic version of paroxetine.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE)