Bipolar Disorder
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Sign up freeTop drugs studied for this disease
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FDA approval · 2018-11-05FDA Approved: GEODON — Supplemental Application (Viatris Specialty LLC)
The FDA approved a supplemental application for Geodon (ziprasidone) submitted by Viatris Specialty LLC.
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FDA approval · 2018-10-04FDA Approved: LITHIUM CARBONATE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for lithium carbonate by Hikma Pharmaceuticals USA Inc. under NDA 017812.
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FDA approval · 2018-10-04FDA Approved: LITHIUM CARBONATE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for Lithium Carbonate submitted by Hikma Pharmaceuticals USA Inc.
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FDA approval · 2018-09-28FDA Approved: QUETIAPINE EXTENDED-RELEASE — Original Application (AlignScience Pharma Inc.)
FDA approved AlignScience Pharma Inc.'s generic extended-release quetiapine tablets (ANDA 209497). The approval enables a generic version of…
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FDA approval · 2018-09-10FDA Approved: CHLORPROMAZINE HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals NY LLC)
FDA approved chlorpromazine hydrochloride under an original application from Amneal Pharmaceuticals; approved indications include schizophre…
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FDA approval · 2018-07-27FDA Approved: RISPERDAL M-TAB — Supplemental Application (Janssen Pharmaceuticals, Inc.)
FDA approved Janssen's supplemental application for RISPERDAL M-TAB (risperidone), resulting in updated labeling or expanded indications for…
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FDA approval · 2018-07-23FDA Approved: LAMICTAL ODT — Supplemental Application (GlaxoSmithKline LLC)
FDA approved a supplemental application for Lamictal ODT (lamotrigine) submitted by GlaxoSmithKline LLC.
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FDA approval · 2018-07-03FDA Approved: OLANZAPINE — Original Application (HEC Pharm USA Inc.)
FDA approved the original Abbreviated New Drug Application for olanzapine (generic) submitted by HEC Pharm USA Inc. The approval enables a g…
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FDA approval · 2018-06-27FDA Approved: LAMICTAL — Supplemental Application (GlaxoSmithKline LLC)
The FDA approved a supplemental application for Lamictal (lamotrigine) submitted by GlaxoSmithKline LLC to update the product labeling.
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FDA approval · 2018-06-27FDA Approved: LAMICTAL ODT — Supplemental Application (GlaxoSmithKline LLC)
The FDA approved a supplemental application for LAMICTAL ODT (lamotrigine) from GlaxoSmithKline LLC. The approval updates the labeling for t…
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FDA approval · 2018-05-03FDA Approved: LITHIUM CARBONATE — Supplemental Application (Glenmark Pharmaceuticals Inc., USA)
The FDA approved a supplemental application for lithium carbonate filed by Glenmark Pharmaceuticals Inc., USA, authorizing changes to the pr…
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FDA approval · 2018-05-03FDA Approved: LITHIUM CARBONATE — Supplemental Application (Camber Pharmaceuticals, Inc.)
FDA approved a supplemental application for lithium carbonate from Camber Pharmaceuticals, Inc. This approval represents an authorized chang…
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FDA approval · 2018-04-30FDA Approved: LITHOBID — Supplemental Application (ANI Pharmaceuticals, Inc.)
FDA approved a supplemental application for LITHOBID (lithium carbonate) by ANI Pharmaceuticals, Inc. under NDA 018027. The action represent…
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FDA approval · 2018-04-18FDA Approved: ARIPIPRAZOLE — Original Application (Dr. Reddy's Laboratories Inc)
The FDA approved Dr. Reddy's Laboratories' generic aripiprazole orally disintegrating tablet through an original ANDA, enabling a generic ve…
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FDA approval · 2018-03-20FDA Approved: TEGRETOL — Supplemental Application (Novartis Pharmaceuticals Corporation)
The FDA approved a supplemental application for Tegretol (carbamazepine) from Novartis Pharmaceuticals Corporation.
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FDA approval · 2018-03-06FDA Approved: DEPAKOTE ER — Supplemental Application (AbbVie Inc.)
The FDA approved a supplemental application for Depakote ER (divalproex sodium) from AbbVie, authorizing changes to its labeling.
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FDA approval · 2018-01-29FDA Approved: LAMOTRIGINE KIT — Supplemental Application (OWP Pharmaceuticals, Inc.)
FDA approved a supplemental application for Lamotrigine Kit from OWP Pharmaceuticals, Inc.
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FDA approval · 2017-12-29FDA Approved: LAMOTRIGINE — Supplemental Application (Alembic Pharmaceuticals Limited)
FDA approves Alembic Pharmaceuticals Limited's supplemental application for lamotrigine chewable dispersible, expanding the approved generic…
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FDA approval · 2017-12-11FDA Approved: ARIPIPRAZOLE — Original Application (Bionpharma Inc.)
FDA approved Bionpharma's ARIPIPRAZOLE as an original application generic, allowing marketing for the same indications as the reference prod…
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FDA approval · 2017-12-04FDA Approved: ARIPIPRAZOLE — Original Application (Solco Healthcare U.S., LLC)
FDA approved ARIPIPRAZOLE from Solco Healthcare U.S., LLC as an original generic application. The approval allows generic aripiprazole for t…
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FDA approval · 2017-11-29FDA Approved: QUETIAPINE — Original Application (Macleods Pharmaceuticals Limited)
FDA approved Macleods Pharmaceuticals Limited's generic quetiapine under an Original Application (ANDA204253), making a generic version of q…
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FDA approval · 2017-11-29FDA Approved: QUETIAPINE FUMARATE — Original Application (Accord Healthcare Inc.)
FDA approved a generic quetiapine fumarate product from Accord Healthcare Inc. under an original ANDA.
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FDA approval · 2017-11-29FDA Approved: QUETIAPINE FUMARATE — Original Application (Ingenus Pharmaceuticals, LLC)
FDA approves Ingenus Pharmaceuticals' quetiapine fumarate under an Original Application, making a generic version of the antipsychotic avail…
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FDA approval · 2017-11-29FDA Approved: QUETIAPINE FUMARATE — Original Application (Aurobindo Pharma Limited)
FDA approved the original application for a generic quetiapine fumarate product from Aurobindo Pharma Limited. Quetiapine is used to treat s…
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FDA approval · 2017-11-29FDA Approved: QUETIAPINE EXTENDED RELEASE — Original Application (ACI Healthcare USA, Inc.)
FDA approved an original application for quetiapine extended-release (generic) by ACI Healthcare USA, Inc., making a generic version of quet…