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FDA approval · 2010-03-25

FDA Approved: PAROXETINE — Supplemental Application (Mylan Pharmaceuticals Inc.)

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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

  • Paroxetine hydrochloride hemihydrate (Paroxetine)

Snippet

SUPPL AP for PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE)