Major Depressive Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2007-06-25FDA Approved: TRAZODONE HYDROCHLORIDE — Supplemental Application (Apotex Corp)
FDA approved Apotex Corp's supplemental application for trazodone hydrochloride (generic), confirming regulatory approval for a change under…
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FDA approval · 2007-06-25FDA Approved: TRAZODONE HYDROCHLORIDE — Supplemental Application (Apotex Corp)
FDA approved a supplemental application for trazodone hydrochloride from Apotex Corp, indicating an approved modification to the product's l…
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FDA approval · 2007-06-25FDA Approved: TRAZODONE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approves a supplemental application for trazodone hydrochloride from Teva Pharmaceuticals USA, Inc.
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FDA approval · 2007-06-13FDA Approved: BUPROPION HYDROCHLORIDE XL — Original Application (Actavis Pharma, Inc.)
FDA approved Actavis Pharma's generic extended-release formulation of bupropion hydrochloride XL under an original ANDA, typically indicated…
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FDA approval · 2007-06-04FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Epic Pharma LLC)
FDA approved a supplemental application for Bupropion Hydrochloride from Epic Pharma LLC, granting regulatory approval of this generic produ…
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FDA approval · 2007-05-24FDA Approved: FLUOXETINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved Teva's supplemental application for fluoxetine, authorizing changes to the product's labeling.
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FDA approval · 2007-05-01FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Bupropion hydrochloride from Aurobindo Pharma Limited, authorizing the generic product under an …
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FDA approval · 2007-04-30FDA Approved: SERTRALINE HYDROCHLORIDE — Original Application (ScieGen Pharmaceuticals Inc)
FDA approved ScieGen Pharmaceuticals Inc.'s sertraline hydrochloride as a generic under an Original Abbreviated New Drug Application for the…
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FDA approval · 2007-04-09FDA Approved: CITALOPRAM — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for a generic formulation of citalopram hydrobromide from Aurobindo Pharma Limited.
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FDA approval · 2007-03-27FDA Approved: CITALOPRAM — Original Application (Torrent Pharmaceuticals Limited)
FDA approved Torrent Pharmaceuticals Limited's original ANDA for Citalopram, a generic antidepressant, indicating approval for use in major …
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FDA approval · 2007-03-26FDA Approved: MIRTAZAPINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for Sun Pharmaceutical Industries' generic mirtazapine.
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FDA approval · 2007-03-15FDA Approved: PROZAC — Supplemental Application (Dista Products Company)
The FDA approved a supplemental application for Prozac (fluoxetine hydrochloride) submitted by Dista Products Company.
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FDA approval · 2007-03-07FDA Approved: PAROXETINE — Original Application (Zydus Lifesciences Limited)
FDA approves Zydus Lifesciences Limited's original application for paroxetine hydrochloride tablets (generic paroxetine). This approval prov…
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FDA approval · 2007-02-09FDA Approved: FLUOXETINE — Original Application (Lannett Company, Inc.)
FDA approved the original application for a generic fluoxetine hydrochloride product from Lannett Company, Inc.
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FDA approval · 2007-02-06FDA Approved: PHENELZINE SULFATE — Supplemental Application (Mylan Pharmaceuticals Inc.)
The FDA approved a supplemental application for phenelzine sulfate submitted by Mylan Pharmaceuticals Inc., indicating regulatory approval o…
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FDA approval · 2007-02-06FDA Approved: SERTRALINE HYDROCHLORIDE — Original Application (Lupin Pharmaceuticals, Inc.)
The FDA approved Lupin Pharmaceuticals' sertraline hydrochloride as a generic drug via an Original ANDA approval.
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FDA approval · 2007-02-06FDA Approved: SERTRALINE HYDROCHLORIDE — Original Application (Quallent Pharmaceuticals Health LLC)
FDA approved an Original Application (ANDA) for sertraline hydrochloride from Quallent Pharmaceuticals Health LLC, a generic version of sert…
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FDA approval · 2007-02-06FDA Approved: SERTRALINE HYDROCHLORIDE — Original Application (Aurobindo Pharma Limited)
The FDA approved an original application for a generic sertraline hydrochloride product from Aurobindo Pharma Limited.
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FDA approval · 2007-02-05FDA Approved: PAROXETINE — Supplemental Application (Apotex Corp.)
FDA approved a supplemental application from Apotex Corp. for paroxetine hydrochloride as a generic product. Paroxetine is used to treat maj…
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FDA approval · 2007-01-29FDA Approved: WELLBUTRIN SR — Supplemental Application (GlaxoSmithKline LLC)
FDA approves a supplemental application for Wellbutrin SR (bupropion hydrochloride) from GlaxoSmithKline LLC.
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FDA approval · 2007-01-25FDA Approved: FLUOXETINE — Supplemental Application (Dr.Reddy's Laboratories Limited)
FDA approved a supplemental application for fluoxetine filed by Dr. Reddy's Laboratories Limited.
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FDA approval · 2006-12-15FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals of New York LLC)
FDA approved an original ANDA for Bupropion hydrochloride from Amneal Pharmaceuticals of New York LLC, providing a generic version of the an…
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FDA approval · 2006-11-30FDA Approved: CITALOPRAM — Original Application (Amneal Pharmaceuticals LLC)
FDA approved Amneal's generic citalopram under an original generic application (ANDA 077289).
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FDA approval · 2006-11-17FDA 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 …
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FDA approval · 2006-10-05FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (BluePoint Laboratories)
FDA approved a supplemental application for Bupropion Hydrochloride generic product by BluePoint Laboratories under an ANDA, updating the ap…