Epilepsy
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Sign up freeTop drugs studied for this disease
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FDA approval · 2015-07-09FDA Approved: VIMPAT — Supplemental Application (UCB, Inc.)
FDA approved a supplemental application for VIMPAT (lacosamide) filed by UCB, Inc.
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FDA approval · 2015-06-25FDA Approved: BANZEL — Supplemental Application (Eisai Inc.)
The FDA approved a supplemental application for BANZEL (rufinamide) submitted by Eisai Inc.
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FDA approval · 2015-06-23FDA Approved: FLUDEOXYGLUCOSE F 18 — Original Application (Jubilant DraxImage Inc., dba Jubilant Radiopharma)
FDA approved the Original Application for Fludeoxyglucose F-18 (FDG F-18) radiopharmaceutical for PET imaging, establishing its labeling and…
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FDA approval · 2015-06-23FDA Approved: FLUDEOXYGLUCOSE F 18 — Original Application (The University of Utah DBA Cyclotron Radiochemistry Lab / Huntsman Cancer Institute)
FDA approved the original application for Fludeoxyglucose F-18 as a radiopharmaceutical imaging agent for PET scans, developed by the Univer…
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FDA approval · 2015-06-19FDA Approved: FYCOMPA — Supplemental Application (Eisai Inc.)
The FDA approved a supplemental application for FYCOMPA (perampanel) from Eisai Inc., resulting in an updated labeling for the drug.
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FDA approval · 2015-06-19FDA Approved: ZONEGRAN — Supplemental Application (Advanz Pharma (US) Corp.)
FDA approved a supplemental application for Zonegran (zonisamide) from Advanz Pharma (US) Corp.
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FDA approval · 2015-06-19FDA Approved: LAMOTRIGINE EXTENDED RELEASE — Supplemental Application (Par Health USA, LLC)
FDA approved a supplemental application for Lamotrigine Extended Release, adding an extended-release formulation to the approved lamotrigine…
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FDA approval · 2015-06-13FDA Approved: ZONISAMIDE — Supplemental Application (Exelan Pharmaceuticals, Inc.)
FDA approved a supplemental application for Zonisamide submitted by Exelan Pharmaceuticals, Inc. under ANDA 077869.
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FDA approval · 2015-06-13FDA Approved: ZONISAMIDE — Supplemental Application (BluePoint Laboratories)
The FDA approved a supplemental application for Zonisamide from BluePoint Laboratories, authorizing a generic version of zonisamide.
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FDA approval · 2015-06-11FDA Approved: APTIOM — Supplemental Application (Sumitomo Pharma America, Inc.)
FDA has approved a Supplemental Application for APTIOM (eslicarbazepine acetate) from Sumitomo Pharma America, expanding labeling/indication…
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FDA approval · 2015-06-10FDA Approved: EXTENDED PHENYTOIN SODIUM — Original Application (Aurobindo Pharma Limited)
FDA approved the Original Application (ANDA204309) for Extended Phenytoin Sodium from Aurobindo Pharma Limited, a generic extended-release f…
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FDA approval · 2015-06-04FDA Approved: LEVETIRACETAM — Original Application (Major Pharmaceuticals)
FDA approved the Original Application for levetiracetam from Major Pharmaceuticals, making a generic version of the anticonvulsant available…
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FDA approval · 2015-05-29FDA Approved: DIVALPROEX SODIUM — Original Application (Amneal Pharmaceuticals LLC)
FDA approved Amneal's generic divalproex sodium product through an Original Application (ANDA 203730).
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FDA approval · 2015-05-21FDA Approved: LEVETIRACETAM — Original Application (Solco healthcare U.S., LLC)
FDA approves the original (generic) application for levetiracetam submitted by Solco Healthcare U.S., LLC.
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FDA approval · 2015-05-18FDA Approved: LEVETIRACETAM — Supplemental Application (Patrin Pharma, Inc.)
The FDA approved a supplemental application for levetiracetam from Patrin Pharma, Inc., indicating regulatory clearance related to an alread…
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FDA approval · 2015-05-18FDA Approved: LAMICTAL — Supplemental Application (GlaxoSmithKline LLC)
The FDA approved a supplemental application for Lamictal (lamotrigine) submitted by GlaxoSmithKline LLC. The action supplements the original…
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FDA approval · 2015-05-18FDA Approved: LAMICTAL ODT — Supplemental Application (GlaxoSmithKline LLC)
FDA approved a supplemental application for Lamictal ODT (lamotrigine) submitted by GlaxoSmithKline LLC. The approval concerns the supplemen…
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FDA approval · 2015-05-08FDA Approved: TROKENDI XR — Supplemental Application (Supernus Pharmaceuticals, Inc.)
The FDA approved a supplemental application for TROKENDI XR (topiramate extended-release) submitted by Supernus Pharmaceuticals, Inc. The ac…
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FDA approval · 2015-05-01FDA Approved: FLUDEOXYGLUCOSE F 18 — Original Application (Biomedical Research Foundation of Northwest Louisiana)
FDA approved Fluorodeoxyglucose F-18 as a diagnostic radiopharmaceutical for positron emission tomography (PET) imaging under an original ap…
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FDA approval · 2015-04-30FDA Approved: DILANTIN-125 — Supplemental Application (Viatris Specialty LLC)
FDA approved a supplemental application for DILANTIN-125 (phenytoin) filed by Viatris Specialty LLC.
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FDA approval · 2015-04-24FDA Approved: ZONISAMIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approves a supplemental application for Zonisamide by Sun Pharmaceutical Industries, Inc., indicating a regulatory modification for the …
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FDA approval · 2015-04-21FDA Approved: NEURONTIN — Supplemental Application (Parke-Davis Div of Pfizer Inc)
FDA approved a supplemental application for Neurontin (gabapentin) submitted by Parke-Davis Div of Pfizer Inc.
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FDA approval · 2015-04-17FDA Approved: GABAPENTIN — Supplemental Application (Advagen Pharma Ltd)
FDA approved a supplemental application for gabapentin submitted by Advagen Pharma Ltd under the existing ANDA. This action updates the regu…
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FDA approval · 2015-04-17FDA Approved: GABAPENTIN — Supplemental Application (Granules Pharmaceuticals Inc)
FDA approved a supplemental application for gabapentin granules from Granules Pharmaceuticals Inc.
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FDA approval · 2015-04-16FDA Approved: DILANTIN — Supplemental Application (Viatris Specialty LLC)
FDA approved a supplemental application for DILANTIN (extended phenytoin sodium), a new extended-release form from Viatris Specialty LLC.