Seasonal Affective Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2010-05-25FDA Approved: WELLBUTRIN SR — Supplemental Application (GlaxoSmithKline LLC)
FDA approved a supplemental application for WELLBUTRIN SR (bupropion hydrochloride) submitted by GlaxoSmithKline LLC, signaling an approved …
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FDA approval · 2010-05-13FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
The FDA approved a supplemental application for Bupropion hydrochloride from Amneal Pharmaceuticals of New York LLC, authorizing a generic v…
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FDA approval · 2010-04-27FDA Approved: BUPROPION HYDROCHLORIDE XL — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for Actavis’s Bupropion Hydrochloride XL, extending regulatory approval for the extended-release for…
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FDA approval · 2010-04-27FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for Bupropion Hydrochloride SR from Actavis Pharma (ANDA), authorizing the continued marketing of th…
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FDA approval · 2010-04-22FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Bupropion hydrochloride tablets from Aurobindo Pharma Limited.
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FDA approval · 2010-04-08FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Aurobindo Pharma Limited)
FDA approved the original ANDA for Bupropion Hydrochloride from Aurobindo Pharma Limited. This approval adds a generic option for the indica…
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FDA approval · 2010-04-06FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical Industries' original application for generic bupropion hydrochloride tablets. The product is indicated for m…
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FDA approval · 2010-04-05FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Epic Pharma LLC)
The FDA approved a supplemental application for Bupropion hydrochloride from Epic Pharma LLC, granting approval for this generic product.
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FDA approval · 2010-02-26FDA Approved: WELLBUTRIN SR — Supplemental Application (GlaxoSmithKline LLC)
The FDA approved a supplemental application for Wellbutrin SR (bupropion hydrochloride) submitted by GlaxoSmithKline LLC, updating the produ…
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FDA approval · 2010-01-27FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for bupropion hydrochloride (generic) submitted by Amneal Pharmaceuticals of New York LLC under ANDA…
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FDA approval · 2010-01-22FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental generic application for BUPROPION HYDROCHLORIDE by Amneal Pharmaceuticals of New York LLC under ANDA077415.
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CLINICAL_TRIALS trial_result · 2010-01-13Clinical Trial Update: Blue Enriched Versus Standard Light Treatment for Seasonal Affective Disorder(SAD) [NA]
A clinical trial comparing blue-enriched light therapy with standard bright light therapy for Seasonal Affective Disorder has completed.
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FDA approval · 2009-12-15FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
The FDA approved Amneal Pharmaceuticals of New York LLC's supplemental application for bupropion hydrochloride, resulting in changes to the …
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FDA approval · 2009-12-15FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for bupropion hydrochloride from Actavis Pharma, confirming approval of a generic version.
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CLINICAL_TRIALS research · 2009-12-11Clinical Trial Update: Bright Light Therapy in Seasonal Affective Disorder (SAD) [NA]
A clinical trial update from the University of Oulu on bright light therapy for Seasonal Affective Disorder, with the trial status listed as…
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FDA approval · 2009-11-16FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for Bupropion Hydrochloride SR from Actavis, a generic sustained-release formulation.
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FDA approval · 2009-11-09FDA Approved: BUPROPION HYDROCHLORIDE XL — Supplemental Application (Actavis Pharma, Inc.)
The FDA approved a supplemental application for Bupropion hydrochloride extended-release (XL) from Actavis Pharma, enabling the generic prod…
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FDA approval · 2009-11-05FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Epic Pharma LLC)
FDA approved a supplemental application for bupropion hydrochloride (Epic Pharma LLC) under ANDA 075932. This approval updates the approved …
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CLINICAL_TRIALS trial_result · 2009-10-05Clinical Trial Update: Ramelteon in the Treatment of Sleep and Mood in Patients With Seasonal Affective Disorder [Phase 4]
Phase 4 trial update assessing ramelteon for sleep and mood in Seasonal Affective Disorder; results were posted in October 2009.
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FDA approval · 2009-07-01FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (BluePoint Laboratories)
FDA approves a supplemental application for Bupropion hydrochloride (ANDA 076143) submitted by BluePoint Laboratories.
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FDA approval · 2009-03-24FDA Approved: BUPROPION HYDROCHLORIDE SR — Original Application (Actavis Pharma, Inc.)
FDA approved a generic sustained-release formulation of bupropion hydrochloride for major depressive disorder and seasonal affective disorde…
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FDA approval · 2008-12-19FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Apnar Pharma LP)
The FDA approved a supplemental application for bupropion hydrochloride submitted by Apnar Pharma LP.
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FDA approval · 2008-11-26FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for a generic Bupropion Hydrochloride product from Amneal Pharmaceuticals of New York LLC, enabling …
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FDA approval · 2008-08-15FDA Approved: BUPROPION HYDROCHLORIDE — Original Application (Actavis Pharma, Inc.)
The FDA approved the original ANDA for bupropion hydrochloride from Actavis Pharma, Inc., enabling a generic product to reach the market. Th…
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FDA approval · 2008-07-10FDA Approved: BUPROPION HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for bupropion hydrochloride from Amneal Pharmaceuticals of New York LLC under ANDA077415.