Panic Disorder

• FDA approval · 2009-10-15
  FDA Approved: CLONAZEPAM — Supplemental Application (Aurobindo Pharma Limited)

  FDA approved a supplemental application for a clonazepam generic product from Aurobindo Pharma Limited.

• FDA approval · 2009-09-30
  FDA Approved: VENLAFAXINE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)

  FDA approved a supplemental application for a generic venlafaxine product manufactured by Heritage Pharmaceuticals (d/b/a Avet Pharmaceutica…

• FDA approval · 2009-09-28
  FDA Approved: FLUOXETINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  The FDA approved a supplemental application for fluoxetine from Teva Pharmaceuticals USA, Inc., updating the approval status of the drug. Th…

• FDA approval · 2009-09-28
  FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Granules Pharmaceuticals Inc.)

  FDA approved the supplemental application for sertraline hydrochloride from Granules Pharmaceuticals Inc., confirming regulatory approval of…

• FDA approval · 2009-09-28
  FDA Approved: FLUOXETINE — Supplemental Application (Chartwell Governmental & Specialty RX, LLC)

  FDA approved a supplemental application for fluoxetine (generic) filed by Chartwell Governmental & Specialty RX, LLC. The approval confirms …

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• FDA approval · 2009-08-31
  FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Quallent Pharmaceuticals Health LLC)

  The FDA approved a supplemental application for sertraline hydrochloride from Quallent Pharmaceuticals Health LLC, enabling the generic prod…

• FDA approval · 2009-08-21
  FDA Approved: FLUOXETINE — Supplemental Application (Dr.Reddy's Laboratories Limited)

  FDA approved a supplemental application for generic fluoxetine from Dr. Reddy's Laboratories Limited.

• FDA approval · 2009-08-07
  FDA Approved: PAXIL — Supplemental Application (Apotex Corp)

  FDA approved a supplemental application from Apotex Corp for Paxil (paroxetine hydrochloride).

• FDA approval · 2009-07-22
  FDA Approved: VENLAFAXINE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  The FDA approved a supplemental application for venlafaxine hydrochloride from Teva Pharmaceuticals USA, Inc. under ANDA076690, authorizing …

• FDA approval · 2009-05-07
  FDA Approved: CLONAZEPAM — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  FDA approved a supplemental application for clonazepam submitted by Teva Pharmaceuticals USA, Inc.

• FDA approval · 2009-04-23
  FDA Approved: KLONOPIN — Supplemental Application (H2-Pharma, LLC)

  FDA approved a supplemental NDA for KLONOPIN (clonazepam) submitted by H2-Pharma, LLC.

• FDA approval · 2009-04-21
  FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Granules Pharmaceuticals Inc.)

  FDA approved a supplemental application for sertraline hydrochloride from Granules Pharmaceuticals Inc., indicating approval of a modificati…

• FDA approval · 2009-04-06
  FDA Approved: VENLAFAXINE HYDROCHLORIDE — Supplemental Application (Dr. Reddy's Laboratories Limited)

  FDA approved a supplemental application for venlafaxine hydrochloride from Dr. Reddy's Laboratories Limited, approving changes related to th…

• FDA approval · 2009-03-19
  FDA Approved: FLUOXETINE — Original Application (Alembic Pharmaceuticals Limited)

  FDA approved the original ANDA for fluoxetine from Alembic Pharmaceuticals Limited, enabling a generic version of fluoxetine to be marketed.

• FDA approval · 2009-03-19
  FDA Approved: FLUOXETINE — Original Application (Aurobindo Pharma Limited)

  FDA approved the original application for Fluoxetine by Aurobindo Pharma Limited, enabling a generic Fluoxetine product. The approved indica…

• FDA approval · 2009-03-06
  FDA Approved: VENLAFAXINE HYDROCHLORIDE — Supplemental Application (Dr. Reddy's Laboratories Limited)

  FDA approved a supplemental application for venlafaxine hydrochloride from Dr. Reddy's Laboratories Limited. This approval authorizes a gene…

• FDA approval · 2009-02-25
  FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)

  FDA approved a supplemental application for sertraline hydrochloride from Aurobindo Pharma Limited, a generic version of the antidepressant …

• FDA approval · 2009-01-30
  FDA Approved: ZOLOFT — Supplemental Application (ROERIG)

  FDA approved a supplemental application for Zoloft (sertraline hydrochloride) submitted by ROERIG.

• FDA approval · 2009-01-30
  FDA Approved: PAROXETINE HYDROCHLORIDE — Supplemental Application (Apotex Corp)

  FDA approved a supplemental application for PAROXETINE HYDROCHLORIDE from Apotex Corp.

• FDA approval · 2009-01-30
  FDA Approved: PAXIL — Supplemental Application (Apotex Corp)

  FDA approved a supplemental application from Apotex Corp for Paxil (paroxetine hydrochloride), authorizing a generic version under the exist…

• FDA approval · 2009-01-30
  FDA Approved: PROZAC — Supplemental Application (Dista Products Company)

  FDA approves a supplemental application for Prozac (fluoxetine hydrochloride) submitted by Dista Products Company.

• FDA approval · 2009-01-27
  FDA Approved: VENLAFAXINE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)

  FDA approved Teva's supplemental application for venlafaxine hydrochloride, enabling marketing of a generic venlafaxine hydrochloride produc…

• FDA approval · 2009-01-09
  FDA Approved: VENLAFAXINE — Original Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)

  FDA approved a generic venlafaxine product under Heritage Pharmaceuticals’ original ANDA, for the treatment of major depressive disorder and…

• FDA approval · 2009-01-09
  FDA Approved: ALPRAZOLAM — Original Application (Par Health USA, LLC)

  The FDA approved ALPRAZOLAM from Par Health USA, LLC under ANDA078088. It represents a generic version of alprazolam for the treatment of an…

• FDA approval · 2008-10-31
  FDA Approved: PAROXETINE HYDROCHLORIDE — Supplemental Application (Apotex Corp)

  FDA approved Apotex Corp's supplemental application for paroxetine hydrochloride (paroxetine HCl), confirming continued approval for the gen…