FDA
approval
· 2010-03-25
FDA Approved: PAROXETINE — Supplemental Application (Mylan Pharmaceuticals Inc.)
Summary
The FDA approved a supplemental application for paroxetine hydrochloride hemihydrate from Mylan Pharmaceuticals Inc., advancing the generic product under ANDA07…
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE)