Obsessive-compulsive Disorder

• FDA approval · 2007-01-25
  FDA Approved: FLUOXETINE — Supplemental Application (Dr.Reddy's Laboratories Limited)

  FDA approved a supplemental application for fluoxetine filed by Dr. Reddy's Laboratories Limited.

• FDA approval · 2006-11-17
  FDA Approved: FLUOXETINE — Supplemental Application (TIME CAP LABORATORIES, INC.)

  The FDA approved a supplemental application for a fluoxetine hydrochloride product from Time Cap Laboratories, Inc., approving this generic …

• FDA approval · 2006-10-18
  FDA Approved: FLUVOXAMINE MALEATE — Supplemental Application (Chartwell RX, LLC)

  FDA approved a supplemental application for fluvoxamine maleate from Chartwell RX, LLC, updating the generic product's approval.

• FDA approval · 2006-08-22
  FDA Approved: PAXIL — Supplemental Application (Apotex Corp)

  The FDA approved a supplemental application for Paxil (paroxetine hydrochloride) submitted by Apotex Corp.

• FDA approval · 2006-08-22
  FDA Approved: PAROXETINE HYDROCHLORIDE — Supplemental Application (Apotex Corp)

  FDA approved a supplemental application for Paroxetine hydrochloride submitted by Apotex Corp.

• Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
• FDA approval · 2006-08-11
  FDA Approved: SERTRALINE — Original Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)

  FDA approved an original application for sertraline (generic) by Heritage Pharmaceuticals d/b/a Avet Pharmaceuticals.

• FDA approval · 2006-07-24
  FDA Approved: FLUVOXAMINE MALEATE — Supplemental Application (Upsher-Smith Laboratories, LLC)

  FDA approved a supplemental application for fluvoxamine maleate, a generic formulation, manufactured by Upsher-Smith Laboratories.

• FDA approval · 2006-07-24
  FDA Approved: FLUVOXAMINE MALEATE — Supplemental Application (Apotex Corp)

  FDA approved a supplemental ANDA for fluvoxamine maleate from Apotex Corp, enabling generic product availability.

• FDA approval · 2006-05-04
  FDA Approved: ZOLOFT — Supplemental Application (ROERIG)

  The FDA approved a supplemental application for Zoloft (sertraline hydrochloride) submitted by Roerig. The approval updates the product's la…