Epilepsy
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Sign up freeTop drugs studied for this disease
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FDA approval · 2008-03-24FDA Approved: DEPAKOTE SPRINKLES — Supplemental Application (AbbVie Inc.)
FDA has approved a supplemental application for Depakote Sprinkles (divalproex sodium) from AbbVie.
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FDA approval · 2008-03-24FDA Approved: DEPAKOTE ER — Supplemental Application (AbbVie Inc.)
FDA approved a supplemental application for Depakote ER (divalproex sodium) submitted by AbbVie. The approval covers changes to Depakote ER'…
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FDA approval · 2008-03-18FDA Approved: FOSPHENYTOIN SODIUM — Original Application (Amneal Pharmaceuticals LLC)
FDA approved Amneal Pharmaceuticals LLC's original application for fosphenytoin sodium (ANDA 078476), establishing a generic option for seiz…
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FDA approval · 2008-03-03FDA Approved: ETHOSUXIMIDE — Supplemental Application (Bionpharma Inc.)
FDA approved a supplemental application for Ethosuximide submitted by Bionpharma Inc. The action updates the regulatory filing for Ethosuxim…
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FDA approval · 2008-02-11FDA Approved: CARBAMAZEPINE — Supplemental Application (Torrent Pharmaceuticals Limited)
FDA approved Torrent Pharmaceuticals Limited's supplemental application for carbamazepine, a generic anticonvulsant. The approval updates th…
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FDA approval · 2008-02-11FDA Approved: CARBAMAZEPINE — Supplemental Application (Torrent Pharmaceuticals Limited)
FDA approved a supplemental application for a generic Carbamazepine product from Torrent Pharmaceuticals Limited (ANDA 077272).
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FDA approval · 2008-01-11FDA Approved: CARBAMAZEPINE — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application for carbamazepine submitted by Chartwell RX, LLC for an existing generic product.
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FDA approval · 2007-12-26FDA Approved: CARBAMAZEPINE — Supplemental Application (Torrent Pharmaceuticals Limited)
FDA approved a supplemental application for carbamazepine from Torrent Pharmaceuticals Limited.
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FDA approval · 2007-12-17FDA Approved: CARBAMAZEPINE — Supplemental Application (Torrent Pharmaceuticals Limited)
The FDA approved Torrent Pharmaceuticals Limited's supplemental application for Carbamazepine, a generic antiepileptic. The action updates t…
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FDA approval · 2007-12-11FDA Approved: TEGRETOL XR — Supplemental Application (Novartis Pharmaceuticals Corporation)
The FDA approved a supplemental application for Tegretol XR (carbamazepine) from Novartis Pharmaceuticals Corporation.
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FDA approval · 2007-12-11FDA Approved: TEGRETOL — Supplemental Application (Novartis Pharmaceuticals Corporation)
The FDA approved a supplemental application for Tegretol (carbamazepine) filed by Novartis Pharmaceuticals Corporation.
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FDA approval · 2007-12-11FDA Approved: OXCARBAZEPINE — Original Application (ANI Pharmaceuticals, Inc.)
The FDA approved ANI Pharmaceuticals' original application for oxcarbazepine, a generic anticonvulsant indicated for partial-onset seizures …
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FDA approval · 2007-10-29FDA Approved: LORAZEPAM — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for Lorazepam from Hikma Pharmaceuticals USA Inc., authorizing the marketing of a Lorazepam product.
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FDA approval · 2007-10-09FDA Approved: OXCARBAZEPINE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical Industries' original application for a generic oxcarbazepine product. This marks approval of a generic versi…
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FDA approval · 2007-10-09FDA Approved: OXCARBAZEPINE — Original Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved the original ANDA for oxcarbazepine from Glenmark Pharmaceuticals.
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FDA approval · 2007-09-12FDA Approved: KEPPRA — Supplemental Application (UCB, Inc.)
FDA approved a supplemental application for Keppra (levetiracetam) submitted by UCB, Inc., resulting in updated labeling/indication as part …
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FDA approval · 2007-09-12FDA Approved: KEPPRA — Supplemental Application (UCB, Inc.)
FDA approved a supplemental application for Keppra (levetiracetam) from UCB, Inc., expanding the product's approved use and/or labeling.
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FDA approval · 2007-09-12FDA Approved: ZONISAMIDE — Supplemental Application (BluePoint Laboratories)
The FDA approved a supplemental application for zonisamide submitted by BluePoint Laboratories. The approval indicates authorization for cha…
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FDA approval · 2007-08-31FDA Approved: TRILEPTAL — Supplemental Application (Novartis Pharmaceuticals Corporation)
The FDA approved a supplemental application for TRILEPTAL (oxcarbazepine) from Novartis Pharmaceuticals Corporation. The action updates labe…
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FDA approval · 2007-08-31FDA Approved: TRILEPTAL — Supplemental Application (Novartis Pharmaceuticals Corporation)
The FDA approved a supplemental application for TRILEPTAL (oxcarbazepine) from Novartis, resulting in a label update for the product.
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FDA approval · 2007-08-16FDA Approved: TEGRETOL XR — Supplemental Application (Novartis Pharmaceuticals Corporation)
FDA approved a supplemental application for Tegretol XR (carbamazepine) submitted by Novartis Pharmaceuticals Corporation.
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FDA approval · 2007-08-16FDA Approved: TEGRETOL — Supplemental Application (Novartis Pharmaceuticals Corporation)
FDA approved a supplemental application for Tegretol (carbamazepine) filed by Novartis Pharmaceuticals Corporation; the approval updates the…
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FDA approval · 2007-08-08FDA Approved: DILANTIN — Supplemental Application (Viatris Specialty LLC)
The FDA approved a supplemental application for Dilantin (extended phenytoin sodium) filed by Viatris Specialty LLC.
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FDA approval · 2007-08-06FDA Approved: FOSPHENYTOIN — Original Application (Fresenius Kabi USA, LLC)
FDA approved the original ANDA for fosphenytoin sodium (FOSPHENYTOIN) by Fresenius Kabi USA, LLC.
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FDA approval · 2007-08-06FDA Approved: FOSPHENYTOIN SODIUM — Original Application (Hikma Pharmaceuticals USA Inc.)
FDA approved the original ANDA for fosphenytoin sodium, a generic version of the anticonvulsant, manufactured by Hikma Pharmaceuticals USA I…