Major Depressive Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2008-02-05FDA Approved: PAROXETINE — Supplemental Application (Apotex Corp.)
FDA approved a supplemental application for Apotex Corp. to market a generic paroxetine hydrochloride product (PAROXETINE HYDROCHLORIDE).
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FDA approval · 2008-01-31FDA Approved: FLUOXETINE — Original Application (QUALLENT PHARMACEUTICALS HEALTH LLC)
FDA approved the original application for a generic fluoxetine hydrochloride product from Quallent Pharmaceuticals Health LLC.
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FDA approval · 2008-01-16FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA granted supplemental approval for Amneal Pharmaceuticals of New York LLC's generic bupropion hydrochloride (ANDA076711). The document in…
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FDA approval · 2008-01-11FDA Approved: SERTRALINE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved a supplemental application for a sertraline generic product from Heritage Pharmaceuticals (Avet), authorizing changes to the ap…
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FDA approval · 2008-01-08FDA Approved: SERTRALINE HYDROCHLORIDE — Original Application (Granules Pharmaceuticals Inc.)
FDA approved Granules Pharmaceuticals Inc.'s sertraline hydrochloride generic under an Original Application. The approval provides a generic…
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FDA approval · 2007-12-26FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for SERTRALINE HYDROCHLORIDE (generic) from Aurobindo Pharma Limited, updating the regulatory status…
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FDA approval · 2007-12-14FDA Approved: EFFEXOR XR — Supplemental Application (Viatris Specialty LLC)
The FDA approved a supplemental application for Effexor XR (venlafaxine hydrochloride) submitted by Viatris Specialty LLC.
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FDA approval · 2007-12-12FDA Approved: TRANYLCYPROMINE SULFATE — Supplemental Application (Strides Pharma Science Limited)
FDA approved a supplemental ANDA for Tranylcypromine Sulfate, enabling Strides Pharma Science Limited to market a generic version of this MA…
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FDA approval · 2007-11-28FDA Approved: DESIPRAMINE HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for desipramine hydrochloride from Actavis Pharma, Inc. This action finalizes the approval of a gene…
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FDA approval · 2007-11-28FDA Approved: DESIPRAMINE HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for desipramine hydrochloride from Actavis Pharma, Inc., signaling an additional approval under an a…
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FDA approval · 2007-11-28FDA Approved: DESIPRAMINE HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for desipramine hydrochloride, authorizing a change to an already approved product filed by Actavis …
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FDA approval · 2007-11-28FDA Approved: DESIPRAMINE HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for desipramine hydrochloride by Actavis Pharma, Inc., approving the generic drug submission.
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FDA approval · 2007-11-26FDA Approved: MIRTAZAPINE — Supplemental Application (Aurolife Pharma LLC)
FDA granted a supplemental approval to Aurolife Pharma LLC for Mirtazapine (generic antidepressant) under an ANDA.
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FDA approval · 2007-11-13FDA Approved: TRAZODONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for trazodone hydrochloride by Sun Pharmaceutical Industries, approving changes to its generic produ…
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FDA approval · 2007-11-07FDA Approved: MIRTAZAPINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved Sun Pharmaceutical Industries' supplemental application for mirtazapine (generic) under an ANDA, authorizing the continued …
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FDA approval · 2007-11-07FDA Approved: PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE — Supplemental Application (Mylan Pharmaceuticals Inc.)
FDA approved a supplemental application for the generic combination product perphenazine and amitriptyline hydrochloride by Mylan Pharmaceut…
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FDA approval · 2007-11-06FDA Approved: MIRTAZAPINE — Supplemental Application (Mylan Pharmaceuticals Inc.)
The FDA approved a supplemental application for Mirtazapine submitted by Mylan Pharmaceuticals Inc., authorizing the generic version of the …
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FDA approval · 2007-11-06FDA Approved: MIRTAZAPINE — Supplemental Application (Apotex Corp.)
The FDA approved a supplemental application submitted by Apotex Corp. for mirtazapine.
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FDA approval · 2007-11-01FDA Approved: CITALOPRAM — Supplemental Application (Mylan Pharmaceuticals Inc.)
The FDA approved a supplemental application for the generic antidepressant Citalopram from Mylan Pharmaceuticals Inc.
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FDA approval · 2007-10-30FDA Approved: MIRTAZAPINE — Supplemental Application (Aurobindo Pharma Limited)
The FDA approved a supplemental application for mirtazapine from Aurobindo Pharma Limited, enabling a regulatory update for this generic ant…
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FDA approval · 2007-10-29FDA Approved: MIRTAZAPINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for the generic antidepressant mirtazapine from Sun Pharmaceutical Industries, Inc., under ANDA 0765…
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FDA approval · 2007-10-29FDA Approved: NEFAZODONE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for nefazodone hydrochloride from Teva Pharmaceuticals USA, Inc.
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FDA approval · 2007-10-25FDA Approved: CITALOPRAM — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Citalopram hydrobromide from Aurobindo Pharma Limited, granting generic approval for their Cital…
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FDA approval · 2007-10-25FDA Approved: CITALOPRAM — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approves a supplemental application for citalopram from Hikma Pharmaceuticals USA Inc., granting approval for its generic antidepressant…
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FDA approval · 2007-10-25FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' supplemental application for sertraline hydrochloride, a generic sertraline product, under the ANDA.