Major Depressive Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2021-09-20FDA Approved: PRISTIQ EXTENDED-RELEASE — Supplemental Application (Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.)
The FDA approved a supplemental application for Pristiq Extended-Release (desvenlafaxine succinate), expanding the product with an extended-…
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FDA approval · 2021-09-20FDA Approved: CELEXA — Supplemental Application (Allergan, Inc.)
FDA approved a supplemental application for Celexa (citalopram) from Allergan, Inc.
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FDA approval · 2021-09-20FDA Approved: VENLAFAXINE HYDROCHLORIDE — Supplemental Application (Dr. Reddy's Laboratories Limited)
FDA approved a supplemental application for venlafaxine hydrochloride from Dr. Reddy's Laboratories Limited.
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FDA approval · 2021-09-20FDA Approved: ESCITALOPRAM OXALATE — Supplemental Application (Rising Pharma Holdings, Inc.)
The FDA approved a supplemental application for a generic escitalopram oxalate product from Rising Pharma Holdings, expanding access to this…
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FDA approval · 2021-09-20FDA Approved: TRINTELLIX — Supplemental Application (Takeda Pharmaceuticals America, Inc.)
The FDA approved a supplemental application for TRINTELLIX (vortioxetine) submitted by Takeda Pharmaceuticals America, Inc.
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FDA approval · 2021-09-20FDA Approved: FLUOXETINE — Supplemental Application (Saptalis Pharmaceuticals, LLC.)
The FDA approved a supplemental application for fluoxetine from Saptalis Pharmaceuticals, LLC., enabling a generic fluoxetine product under …
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FDA approval · 2021-09-20FDA Approved: FLUOXETINE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for fluoxetine from Aurobindo Pharma Limited, granting approval of a generic fluoxetine product.
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FDA approval · 2021-09-20FDA Approved: VENLAFAXINE HYDROCHLORIDE — Supplemental Application (Vertical Pharmaceuticals, LLC)
The FDA approved a supplemental application for Venlafaxine hydrochloride from Vertical Pharmaceuticals, LLC.
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FDA approval · 2021-09-20FDA Approved: FLUOXETINE HYDROCHLORIDE — Supplemental Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' supplemental application for fluoxetine hydrochloride, enabling marketing of a generic fluoxetine produc…
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FDA approval · 2021-09-13FDA Approved: CITALOPRAM — Supplemental Application (Chartwell Governmental & Specialty RX, LLC.)
The FDA approved a supplemental application for citalopram filed by Chartwell Governmental & Specialty RX, LLC.
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FDA approval · 2021-09-13FDA Approved: CITALOPRAM HYDROBROMIDE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Aurobindo Pharma Limited's generic citalopram hydrobromide, expanding its approved product to ma…
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FDA approval · 2021-09-08FDA Approved: ESCITALOPRAM ORAL SOLUTION — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application for escitalopram oral solution, adding an approved oral solution formulation for the antidepressant …
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FDA approval · 2021-09-08FDA Approved: ESCITALOPRAM — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for escitalopram oxalate from Sun Pharmaceutical Industries, Inc., indicating approval of a gene…
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FDA approval · 2021-09-03FDA Approved: VENLAFAXINE — Supplemental Application (Cadila Pharmaceuticals Limited)
FDA approved a supplemental application for Venlafaxine from Cadila Pharmaceuticals Limited.
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FDA approval · 2021-09-03FDA Approved: VENLAFAXINE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved a supplemental application for venlafaxine (generic) from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., approv…
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FDA approval · 2021-09-03FDA Approved: PAROXETINE — Original Application (ANI Pharmaceuticals, Inc.)
ANI Pharmaceuticals received FDA approval for an original ANDA application for paroxetine, a generic antidepressant.
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FDA approval · 2021-09-02FDA Approved: VENLAFAXINE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for venlafaxine by Sun Pharmaceutical Industries, Inc.
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FDA approval · 2021-09-01FDA Approved: FLUOXETINE HYDROCHLORIDE — Supplemental Application (Dr.Reddy's Laboratories Limited)
FDA approved a supplemental application for fluoxetine hydrochloride from Dr. Reddy's Laboratories Limited (ANDA 078572), updating regulator…
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FDA approval · 2021-08-31FDA Approved: FLUOXETINE — Supplemental Application (Saptalis Pharmaceuticals, LLC.)
FDA approved a supplemental application for fluoxetine from Saptalis Pharmaceuticals, confirming the availability of a generic fluoxetine pr…
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FDA approval · 2021-08-27FDA Approved: FLUOXETINE — Supplemental Application (PAI Holdings, LLC dba PAI Pharma)
FDA approved a supplemental application for a fluoxetine hydrochloride generic product from PAI Holdings (PAI Pharma). This action approves …
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FDA approval · 2021-08-27FDA Approved: PAROXETINE — Original Application (Modavar Pharmaceuticals LLC)
FDA approved a generic paroxetine tablet product from Modavar Pharmaceuticals LLC under an original abbreviated new drug application (ANDA 2…
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FDA approval · 2021-08-25FDA Approved: FLUOXETINE — Supplemental Application (Dr.Reddy's Laboratories Limited)
The FDA approved a supplemental application for Fluoxetine from Dr. Reddy's Laboratories Limited.
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FDA approval · 2021-08-23FDA Approved: CLOMIPRAMINE HYDROCHLORIDE — Supplemental Application (Northstar Rx LLC.)
FDA approved a supplemental application for clomipramine hydrochloride from Northstar Rx LLC., enabling the generic product's continued regu…
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FDA approval · 2021-08-16FDA Approved: MIRTAZAPINE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for a generic Mirtazapine product from Aurobindo Pharma Limited, enabling continued marketing of an …
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FDA approval · 2021-08-06FDA Approved: VENLAFAXINE HYDROCHLORIDE — Original Application (Epic Pharma, LLC)
FDA approved the original application for Venlafaxine hydrochloride (generic) manufactured by Epic Pharma, LLC.