Migraine
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Sign up freeTop drugs studied for this disease
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FDA approval · 2024-01-04FDA Approved: TROKENDI XR — Supplemental Application (Supernus Pharmaceuticals, Inc.)
The FDA approved a supplemental application for TROKENDI XR (topiramate) filed by Supernus Pharmaceuticals, Inc., updating the product's lab…
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FDA approval · 2024-01-04FDA Approved: TOPIRAMATE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Topiramate from Aurobindo Pharma Limited under an ANDA for an already approved generic product.
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FDA approval · 2023-12-27FDA Approved: DIVALPROEX SODIUM — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for divalproex sodium from Aurobindo Pharma Limited under an ANDA.
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FDA approval · 2023-12-15FDA Approved: BUTALBITAL, ASPIRIN, CAFFEINE AND CODEINE PHOSPHATE — Supplemental Application (Amneal Pharmaceuticals of New York, LLC)
The FDA approved a supplemental application for Amneal's fixed-dose combination product of butalbital, aspirin, caffeine and codeine phospha…
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FDA approval · 2023-12-05FDA Approved: TOPIRAMATE — Original Application (Upsher-Smith Laboratories, LLC)
FDA approves an original abbreviated application for Topiramate from Upsher-Smith Laboratories, establishing a generic formulation of the an…
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FDA approval · 2023-11-22FDA Approved: DIVALPROEX SODIUM — Supplemental Application (Bionpharma Inc.)
FDA approved a supplemental application for divalproex sodium submitted by Bionpharma Inc. under an ANDA.
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FDA approval · 2023-11-17FDA Approved: TOPIRAMATE — Original Application (Dr. Reddys Laboratories Inc.)
FDA approves a generic version of Topiramate from Dr. Reddy's Laboratories Inc. through an Original Application (ANDA).
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FDA approval · 2023-11-07FDA Approved: INDERAL LA — Supplemental Application (ANI Pharmaceuticals, Inc.)
FDA approved a supplemental application for Inderal LA (propranolol hydrochloride) by ANI Pharmaceuticals, Inc. The action confirms regulato…
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FDA approval · 2023-10-23FDA Approved: DIVALPROEX SODIUM — Supplemental Application (Mylan Pharmaceuticals Inc.)
FDA approved a supplemental application for divalproex sodium from Mylan Pharmaceuticals, indicating regulatory authorization for a generic …
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FDA approval · 2023-10-06FDA Approved: DIVALPROEX SODIUM — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for divalproex sodium from Sun Pharmaceutical Industries, Inc.
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FDA approval · 2023-10-06FDA Approved: DIVALPROEX SODIUM — Supplemental Application (Upsher-Smith Laboratories, LLC)
FDA approved a supplemental application for divalproex sodium from Upsher-Smith Laboratories, LLC.
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FDA approval · 2023-09-27FDA Approved: TOPIRAMATE — Original Application (Aurobindo Pharma Limited)
FDA approves the Original Application for Topiramate (generic) by Aurobindo Pharma Limited. Topiramate is used as an anticonvulsant for epil…
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FDA approval · 2023-09-26FDA Approved: DIVALPROEX SODIUM — Original Application (Camber Pharmaceuticals, Inc.)
FDA approved Camber Pharmaceuticals' original ANDA for divalproex sodium, providing a generic option for this anticonvulsant/mood stabilizer…
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FDA approval · 2023-09-12FDA Approved: DIHYDROERGOTAMINE MESYLATE NASAL — Supplemental Application (Cipla USA Inc.)
FDA approved Cipla's dihydroergotamine mesylate nasal product via a supplemental application, enabling its marketed use in the United States…
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FDA approval · 2023-08-18FDA Approved: DIHYDROERGOTAMINE MESYLATE — Original Application (Gland Pharma Limited)
FDA approved the original application for dihydroergotamine mesylate from Gland Pharma Limited. This represents the approval of a generic pr…
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FDA approval · 2023-08-15FDA Approved: TOPIRAMATE — Original Application (Ajanta Pharma USA Inc.)
The FDA approved Ajanta Pharma USA Inc.'s generic Topiramate through an Original Application (ANDA 215663). This approval provides a generic…
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FDA approval · 2023-08-07FDA Approved: TOPIRAMATE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for Topiramate submitted by Zydus Lifesciences Limited.
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FDA approval · 2023-07-31FDA Approved: DIVALPROEX SODIUM — Supplemental Application (Lupin Pharmaceuticals, Inc.)
FDA approved a supplemental application for divalproex sodium by Lupin Pharmaceuticals, Inc. under ANDA 078790.
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FDA approval · 2023-07-28FDA Approved: DIVALPROEX SODIUM — Supplemental Application (BluePoint Laboratories)
FDA approved a supplemental application for divalproex sodium submitted by BluePoint Laboratories, associated with an existing ANDA.
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FDA approval · 2023-07-17FDA Approved: TOPIRAMATE — Supplemental Application (Camber Pharmaceuticals, Inc.)
The FDA approved Camber Pharmaceuticals' supplemental application for Topiramate (generic).
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FDA approval · 2023-06-22FDA Approved: DIHYDROERGOTAMINE MESYLATE — Original Application (Advagen Pharma Ltd)
FDA approved an original application for dihydroergotamine mesylate from Advagen Pharma Ltd, establishing this product as a new approved opt…
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FDA approval · 2023-06-07FDA Approved: RIZATRIPTAN — Supplemental Application (Macleods Pharmaceuticals Limited)
FDA approved a supplemental application for rizatriptan submitted by Macleods Pharmaceuticals Limited.
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FDA approval · 2023-06-07FDA Approved: RIZATRIPTAN BENZOATE — Supplemental Application (Macleods Pharmaceuticals Limited)
The FDA approved a supplemental application for rizatriptan benzoate submitted by Macleods Pharmaceuticals Limited. It concerns a supplement…
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FDA approval · 2023-06-06FDA Approved: SUMATRIPTAN SUCCINATE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for sumatriptan succinate submitted by Sun Pharmaceutical Industries, Inc.
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FDA approval · 2023-05-15FDA Approved: EXCEDRIN MIGRAINE GELTABS — Supplemental Application (Haleon US Holdings LLC)
The FDA approved a supplemental application for Excedrin Migraine Geltabs, adding a gelatin-based tablet form of the product that contains a…