Major Depressive Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2017-11-03FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Dr. Reddys Laboratories Inc.)
FDA approved a supplemental application for Bupropion Hydrochloride SR from Dr. Reddy's Laboratories Inc., enabling the generic product's ma…
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FDA approval · 2017-11-03FDA Approved: BUPROPION HYDROCHLORIDE (XL) — Original Application (Upsher-Smith Laboratories, LLC)
FDA approved a new original application for Bupropion Hydrochloride Extended-Release (XL) by Upsher-Smith Laboratories, LLC, enabling generi…
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FDA approval · 2017-10-10FDA Approved: TRAZODONE HYDROCHLORIDE — Original Application (Zydus Lifesciences Limited)
The FDA approved the original application for trazodone hydrochloride by Zydus Lifesciences Limited, enabling the marketing of a generic tra…
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FDA approval · 2017-10-06FDA Approved: AMITRIPTYLINE HYDROCHLORIDE — Original Application (Northstar Rx LLC.)
FDA approved an original application for amitriptyline hydrochloride (generic) from Northstar Rx LLC, authorizing its use as an approved gen…
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FDA approval · 2017-10-05FDA Approved: VENLAFAXINE HYDROCHLORIDE — Original Application (Macleods Pharmaceuticals Limited)
FDA approves Macleods Pharmaceuticals Limited's venlafaxine hydrochloride original application (generic), expanding access to treatment for …
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FDA approval · 2017-09-26FDA 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.
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FDA approval · 2017-09-26FDA Approved: QUETIAPINE FUMARATE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for quetiapine fumarate from Sun Pharmaceutical Industries, Inc., approving updates to the generic's…
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FDA approval · 2017-09-26FDA Approved: QUETIAPINE FUMARATE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application to market a generic quetiapine fumarate product from Aurobindo Pharma Limited.
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FDA approval · 2017-09-08FDA Approved: TRAZODONE HYDROCHLORIDE — Original Application (Accord Healthcare, Inc.)
FDA approved Accord Healthcare's original application for trazodone hydrochloride tablets, establishing a generic version of trazodone hydro…
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FDA approval · 2017-08-18FDA Approved: PAROXETINE — Original Application (Solco Healthcare LLC)
FDA approves the original generic application for Paroxetine (Solco Healthcare LLC).
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FDA approval · 2017-08-11FDA Approved: WELLBUTRIN SR — Supplemental Application (GlaxoSmithKline LLC)
FDA approved a supplemental application for Wellbutrin SR (bupropion hydrochloride) filed by GlaxoSmithKline LLC, updating the product label…
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FDA approval · 2017-08-04FDA Approved: ARIPIPRAZOLE — Supplemental Application (Quallent Pharmaceuticals Health LLC)
The FDA approved a supplemental application for aripiprazole by Quallent Pharmaceuticals Health LLC, bringing a generic version of the antip…
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FDA approval · 2017-08-03FDA Approved: SERTRALINE HYDROCHLORIDE — Supplemental Application (Rising Pharma Holdings, Inc.)
FDA approved a supplemental application for Sertraline Hydrochloride submitted by Rising Pharma Holdings, Inc.
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FDA approval · 2017-07-14FDA Approved: EMSAM — Supplemental Application (Viatris Specialty LLC)
FDA approved a supplemental application for EMSAM (selegiline) by Viatris Specialty LLC.
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FDA approval · 2017-07-03FDA Approved: QUETIAPINE FUMARATE — Supplemental Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved a supplemental application for quetiapine fumarate filed by Unichem Pharmaceuticals (USA), Inc.
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FDA approval · 2017-06-30FDA Approved: QUETIAPINE — Supplemental Application (Accord Healthcare Inc.)
FDA approved a supplemental application for quetiapine from Accord Healthcare Inc. (ANDA 202152).
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FDA approval · 2017-06-30FDA Approved: QUETIAPINE FUMARATE — Supplemental Application (BluePoint Laboratories)
FDA approved a supplemental application for quetiapine fumarate (Quetiapine) by BluePoint Laboratories under an existing ANDA. This represen…
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FDA approval · 2017-06-30FDA Approved: BUPROPION HYDROCHLORIDE SR — Supplemental Application (Actavis Pharma, Inc.)
The FDA approved a supplemental application for Bupropion Hydrochloride SR from Actavis Pharma, Inc., granting approval of a generic sustain…
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FDA approval · 2017-06-30FDA Approved: BUPROPION HYDROCHLORIDE (SR) — Supplemental Application (ScieGen Pharmaceuticals, Inc.)
The FDA approved a supplemental application for Bupropion hydrochloride sustained-release from ScieGen Pharmaceuticals, Inc. (ANDA 206122). …
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FDA approval · 2017-06-30FDA Approved: BUPROPION HYDROCHLORIDE XL — Original Application (Epic Pharma, LLC)
FDA approves Epic Pharma's generic bupropion hydrochloride extended-release tablets (Bupropion HCl XL) under an Original Application, adding…
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FDA approval · 2017-06-30FDA Approved: QUETIAPINE FUMARATE — Supplemental Application (Alembic Pharmaceuticals Limited)
The FDA approved a supplemental application for a generic quetiapine fumarate by Alembic Pharmaceuticals Limited.
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FDA approval · 2017-06-30FDA Approved: QUETIAPINE FUMARATE — Supplemental Application (Macleods Pharmaceuticals Limited)
FDA approved a supplemental application for Macleods Pharmaceuticals Limited to market quetiapine fumarate. The approval covers a generic ve…
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FDA approval · 2017-06-28FDA Approved: DOXEPIN HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals NY LLC)
FDA approved the Original Application for doxepin hydrochloride by Amneal Pharmaceuticals NY LLC, confirming approval of this generic produc…
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FDA approval · 2017-06-22FDA Approved: QUETIAPINE FUMARATE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for quetiapine fumarate by Hikma Pharmaceuticals USA Inc., representing a new or updated approval fo…
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FDA approval · 2017-06-15FDA Approved: ZOLOFT — Supplemental Application (ROERIG)
FDA approved a supplemental application for ZOLOFT (sertraline hydrochloride) submitted by ROERIG, indicating an approved modification to th…