Migraine
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Sign up freeTop drugs studied for this disease
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FDA approval · 2009-09-30FDA Approved: TOPIRAMATE — Supplemental Application (Cipla USA Inc.)
FDA approved a supplemental application for Topiramate from Cipla USA Inc., reflecting an approved supplemental change to a previously autho…
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FDA approval · 2009-08-10FDA Approved: SUMATRIPTAN — Original Application (Bionpharma Inc.)
FDA approved Bionpharma Inc.'s generic Sumatriptan via an Original Application (ANDA) for the treatment of acute migraine in adults.
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FDA approval · 2009-08-10FDA Approved: SUMATRIPTAN — Original Application (SUN PHARMACEUTICAL INDUSTRIES, INC.)
The FDA approved Sun Pharmaceutical Industries' original ANDA for sumatriptan, a generic tablet indicated for the acute treatment of migrain…
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FDA approval · 2009-08-10FDA Approved: SUMATRIPTAN SUCCINATE — Original Application (Dr. Reddy's Laboratories Limited)
FDA approved the original application for Sumatriptan succinate from Dr. Reddy's Laboratories Limited, granting a generic version of sumatri…
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FDA approval · 2009-08-10FDA Approved: SUMATRIPTAN — Original Application (Aurobindo Pharma Limited)
FDA approved the original application for sumatriptan succinate from Aurobindo Pharma Limited through an ANDA, confirming a generic product …
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FDA approval · 2009-08-10FDA Approved: SUMATRIPTAN SUCCINATE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical's generic sumatriptan succinate under an Original Application for the acute treatment of migraine with or wi…
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FDA approval · 2009-08-10FDA Approved: SUMATRIPTAN SUCCINATE — Original Application (Mylan Pharmaceuticals Inc.)
FDA approves Mylan's original application for sumatriptan succinate, a generic product for the acute treatment of migraine.
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FDA approval · 2009-08-04FDA Approved: DIVALPROEX SODIUM — Supplemental Application (BluePoint Laboratories)
FDA has approved a supplemental application for divalproex sodium from BluePoint Laboratories.
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FDA approval · 2009-03-27FDA Approved: TOPIRAMATE — Original Application (Aurobindo Pharma Limited)
FDA approved Aurobindo Pharma Limited's Original Application for Topiramate, granting a generic version of the anticonvulsant Topiramate. Th…
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FDA approval · 2009-03-27FDA Approved: TOPIRAMATE — Original Application (Cipla USA Inc.)
FDA approved Cipla USA Inc.'s generic Topiramate through an original ANDA.
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FDA approval · 2009-03-27FDA Approved: TOPIRAMATE — Original Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved Glenmark's original ANDA for topiramate, enabling a generic version of the anticonvulsant and migraine preventive drug.
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FDA approval · 2009-03-27FDA Approved: TOPIRAMATE — Original Application (Zydus Lifesciences Limited)
FDA approved a generic Topiramate product (Original Application) from Zydus Lifesciences Limited.
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FDA approval · 2009-03-27FDA Approved: TOPIRAMATE — Original Application (Cipla USA Inc.)
FDA approval of a generic Topiramate product from Cipla USA Inc. (Original Application).
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FDA approval · 2009-03-27FDA Approved: TOPIRAMATE — Original Application (Unichem Pharmaceuticals (USA), Inc.)
The FDA approved Unichem Pharmaceuticals (USA), Inc.'s original application for a generic Topiramate product, expanding access to this anti-…
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FDA approval · 2009-03-27FDA Approved: TOPIRAMATE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical's Original Application for Topiramate, enabling the generic Topiramate to be marketed.
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FDA approval · 2009-03-02FDA Approved: SUMATRIPTAN SUCCINATE — Original Application (Fresenius Kabi USA, LLC)
FDA approved Fresenius Kabi USA, LLC's sumatriptan succinate as an Original Application (ANDA), establishing a generic equivalent for treati…
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FDA approval · 2009-02-27FDA Approved: DIVALPROEX SODIUM — Original Application (BluePoint Laboratories)
FDA approved the original application for divalproex sodium (generic) by BluePoint Laboratories.
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FDA approval · 2009-02-09FDA Approved: SUMATRIPTAN — Original Application (SUN PHARMACEUTICAL INDUSTRIES, INC.)
FDA approves Sun Pharmaceutical Industries' original application for Sumatriptan (oral tablet), a generic treatment for acute migraine in ad…
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FDA approval · 2009-01-27FDA Approved: DIVALPROEX SODIUM — Original Application (Zydus Pharmaceuticals USA Inc.)
FDA approved an original application for a generic divalproex sodium product from Zydus Pharmaceuticals USA Inc.
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FDA approval · 2009-01-23FDA Approved: DIVALPROEX SODIUM — Original Application (NorthStar Rx LLC)
The FDA approved NorthStar Rx LLC's original application for divalproex sodium (generic).
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FDA approval · 2008-12-01FDA Approved: BUTALBITAL, ACETAMINOPHEN AND CAFFEINE — Original Application (Granules Pharmaceuticals Inc.)
FDA approved Granules Pharmaceuticals Inc. for a generic version of Butalbital, Acetaminophen and Caffeine (Butalbital/Acetaminophen/Caffein…
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FDA approval · 2008-11-25FDA Approved: DIVALPROEX SODIUM — Original Application (Bionpharma Inc.)
FDA approved Bionpharma's original application for divalproex sodium, making a generic version available for epilepsy, bipolar disorder, and…
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FDA approval · 2008-10-14FDA Approved: ZOMIG — Supplemental Application (Amneal Pharmaceuticals LLC)
The FDA approved a supplemental application for ZOMIG (zolmitriptan) submitted by Amneal Pharmaceuticals LLC.
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FDA approval · 2008-07-29FDA Approved: DIVALPROEX SODIUM — Original Application (Lupin Pharmaceuticals, Inc.)
FDA approved Lupin Pharmaceuticals' generic divalproex sodium (Original Application), enabling a generic version of the reference product.
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FDA approval · 2008-07-29FDA Approved: DIVALPROEX SODIUM — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical Industries' divalproex sodium as an original ANDA (generic) application.