Migraine
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Sign up freeTop drugs studied for this disease
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FDA approval · 2011-07-07FDA Approved: TOPIRAMATE — Supplemental Application (Aurobindo Pharma Limited)
FDA approved a supplemental application for Topiramate by Aurobindo Pharma Limited under an ANDA.
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FDA approval · 2011-06-27FDA Approved: TOPAMAX — Supplemental Application (Janssen Pharmaceuticals, Inc.)
FDA approved a supplemental application for TOPAMAX (topiramate) filed by Janssen Pharmaceuticals, Inc., to update/expand the approved label…
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FDA approval · 2011-06-24FDA Approved: TOPIRAMATE — Supplemental Application (Cipla USA Inc.)
The FDA approved a supplemental application for TOPIRAMATE (Cipla USA Inc.), authorizing changes to the product labeling under the ANDA.
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FDA approval · 2011-06-24FDA Approved: TOPIRAMATE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for Topiramate by Zydus Lifesciences Limited.
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FDA approval · 2011-06-24FDA Approved: TOPIRAMATE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for Topiramate from Zydus Lifesciences Limited, updating the approved generic Topiramate product. Th…
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FDA approval · 2011-06-22FDA Approved: BUTALBITAL, ACETAMINOPHEN AND CAFFEINE — Supplemental Application (Chartwell RX, LLC)
The FDA approved a supplemental application for the analgesic combination butalbital/acetaminophen/caffeine from Chartwell RX, LLC.
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FDA approval · 2011-06-22FDA Approved: BUTALBITAL AND ACETAMINOPHEN — Supplemental Application (Endo USA)
FDA approved a supplemental application for butalbital and acetaminophen (Endo USA), approving changes to the product's labeling.
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FDA approval · 2011-06-22FDA Approved: BUTALBITAL, ACETAMINOPHEN AND CAFFEINE — Supplemental Application (Mayne Pharma)
FDA approves the supplemental application for the generic combination of butalbital, acetaminophen and caffeine manufactured by Mayne Pharma…
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FDA approval · 2011-06-21FDA Approved: SUMATRIPTAN SUCCINATE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical's sumatriptan succinate as an original ANDA, granting generic approval for this migraine treatment.
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FDA approval · 2011-05-12FDA Approved: SUMATRIPTAN — Supplemental Application (Aurobindo Pharma Limited)
The FDA approved a supplemental application for a Sumatriptan succinate generic product from Aurobindo Pharma Limited under ANDA 078327. Thi…
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FDA approval · 2011-04-13FDA Approved: RELPAX — Supplemental Application (ROERIG)
FDA approved a supplemental application for RELPAX (eletriptan hydrobromide) submitted by Roerig.
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FDA approval · 2011-04-05FDA Approved: DIVALPROEX SODIUM — Original Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved the generic divalproex sodium from Unichem Pharmaceuticals (USA), Inc. under ANDA079163.
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FDA approval · 2011-03-17FDA Approved: INDERAL LA — Supplemental Application (ANI Pharmaceuticals, Inc.)
FDA approved a supplemental application for Inderal LA (propranolol hydrochloride) filed by ANI Pharmaceuticals, Inc.
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FDA approval · 2011-02-28FDA Approved: NARATRIPTAN — Original Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved a generic naratriptan product from Heritage Pharmaceuticals (d/b/a Avet Pharmaceuticals) under an ANDA for the acute treatment …
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FDA approval · 2011-02-18FDA Approved: SUMATRIPTAN — Supplemental Application (SUN PHARMACEUTICAL INDUSTRIES, INC.)
The FDA approved a supplemental application for Sumatriptan from Sun Pharmaceutical Industries, Inc. under its ANDA.
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FDA approval · 2011-02-18FDA Approved: SUMATRIPTAN — Supplemental Application (SUN PHARMACEUTICAL INDUSTRIES, INC.)
FDA approved a supplemental application for Sumatriptan from Sun Pharmaceutical Industries, Inc., for the marketed product used to treat acu…
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FDA approval · 2011-01-25FDA Approved: VALPROIC ACID — Supplemental Application (Bionpharma Inc.)
FDA approved a supplemental application for Valproic acid submitted by Bionpharma Inc.
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FDA approval · 2011-01-21FDA Approved: DIVALPROEX SODIUM — Supplemental Application (NorthStar Rx LLC)
FDA approved a supplemental application for divalproex sodium submitted by NorthStar Rx LLC.
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FDA approval · 2010-12-28FDA Approved: TOPIRAMATE — Supplemental Application (Cipla USA Inc.)
FDA approved Cipla USA Inc.'s supplemental application for Topiramate under ANDA 079162 for the generic product.
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FDA approval · 2010-12-28FDA Approved: TOPIRAMATE — Supplemental Application (Unichem Pharmaceuticals (USA), Inc.)
The FDA approved the supplemental application for Topiramate submitted by Unichem Pharmaceuticals (USA), Inc., under ANDA090162.
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FDA approval · 2010-12-23FDA Approved: TOPIRAMATE — Supplemental Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved a supplemental application for TOPIRAMATE SPINKLE, a sprinkle formulation of topiramate manufactured by Heritage Pharmaceutical…
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FDA approval · 2010-12-10FDA Approved: IBUPROFEN — Original Application (Dolgencorp, Inc.)
FDA approved Dolgencorp, Inc.'s ibuprofen 200 mg tablets as an original generic application (ANDA). The approval supports OTC use for relief…
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FDA approval · 2010-12-03FDA Approved: PROCHLORPERAZINE EDISYLATE — Supplemental Application (Civica, Inc.)
FDA approved a supplemental application for Prochlorperazine edisylate from Civica, Inc. to update the labeling per the supplement. The appr…
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FDA approval · 2010-11-22FDA Approved: DG HEALTH MIGRAINE RELIEF — Supplemental Application (Dolgencorp, LLC)
The FDA approved a supplemental application for DG HEALTH MIGRAINE RELIEF by Dolgencorp, LLC. The product combines acetaminophen, aspirin, a…
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FDA approval · 2010-08-13FDA Approved: TOPIRAMATE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for Topiramate from Zydus Lifesciences Limited, indicating an update to the generic's labeling post-…