FDA
approval
· 2023-03-23
FDA Approved: PAROXETINE — Supplemental Application (Modavar Pharmaceuticals LLC)
Summary
FDA approved a supplemental application for generic paroxetine filed by Modavar Pharmaceuticals LLC under ANDA212645.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for PAROXETINE (PAROXETINE)