Ventricular Tachycardia
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Sign up freeTop drugs studied for this disease
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FDA approval · 2012-01-11FDA Approved: SOTALOL HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved Teva Pharmaceuticals USA, Inc.'s supplemental application for sotalol hydrochloride, confirming approval of a generic product. …
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FDA approval · 2011-12-12FDA Approved: NEXTERONE — Supplemental Application (Baxter Healthcare Company)
FDA approved a supplemental application for NEXTERONE (amiodarone hydrochloride) from Baxter Healthcare Company.
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FDA approval · 2011-08-17FDA Approved: BETAPACE — Supplemental Application (Legacy Pharma USA, Inc.)
FDA approved a supplemental application for BETAPACE (sotalol hydrochloride) from Legacy Pharma USA, Inc.
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FDA approval · 2011-04-28FDA Approved: SOTALOL HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for Sotalol Hydrochloride by Teva Pharmaceuticals USA, Inc.
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FDA approval · 2011-02-03FDA Approved: BETAPACE — Supplemental Application (Legacy Pharma USA, Inc.)
FDA approved a supplemental application for BETAPACE (sotalol hydrochloride) submitted by Legacy Pharma USA, Inc., resulting in updated labe…
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FDA approval · 2010-08-31FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Zydus Lifesciences Limited)
FDA approved a supplemental application for amiodarone hydrochloride from Zydus Lifesciences Limited, authorizing the continued marketing of…
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FDA approval · 2010-02-04FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for amiodarone hydrochloride from Sun Pharmaceutical Industries, approving the supplemental filing f…
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FDA approval · 2010-02-04FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for amiodarone hydrochloride from Sun Pharmaceutical Industries, Inc.
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FDA approval · 2009-12-01FDA Approved: PACERONE — Supplemental Application (Upsher-Smith Laboratories, LLC)
FDA approved a supplemental application for PACERONE (amiodarone hydrochloride) by Upsher-Smith Laboratories, LLC, indicating a labeling or …
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FDA approval · 2009-11-20FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Gland Pharma Limited)
FDA approved a supplemental application for amiodarone hydrochloride from Gland Pharma Limited.
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FDA approval · 2009-07-10FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for amiodarone hydrochloride by Hikma Pharmaceuticals USA Inc., granting continued/updated approval …
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FDA approval · 2009-07-09FDA Approved: FLECAINIDE ACETATE — Original Application (Chartwell RX, LLC)
FDA approved flecainide acetate under an Original Application (ANDA) for Chartwell RX, LLC, enabling a generic version of this antiarrhythmi…
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FDA approval · 2009-07-02FDA Approved: SOTALOL HYDROCHLORIDE — Original Application (ALTATHERA Pharmaceuticals, LLC)
FDA approved ALTATHERA Pharmaceuticals' original application for sotalol hydrochloride, a beta-blocker used to manage certain arrhythmias.
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FDA approval · 2009-06-02FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for amiodarone hydrochloride from Sun Pharmaceutical Industries, Inc.
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FDA approval · 2009-06-02FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for amiodarone hydrochloride from Sun Pharmaceutical Industries, Inc., granting additional regulator…
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FDA approval · 2009-01-15FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Gland Pharma Limited)
FDA approved a supplemental application for amiodarone hydrochloride from Gland Pharma Limited, approving this generic product for marketing…
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FDA approval · 2008-12-24FDA Approved: NEXTERONE — Original Application (Baxter Healthcare Company)
FDA approved NEXTERONE (amiodarone hydrochloride) injection under an original NDA for Baxter Healthcare Company. It is indicated for the tre…
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FDA approval · 2008-12-05FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for amiodarone hydrochloride submitted by Sun Pharmaceutical Industries, Inc.
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FDA approval · 2008-12-05FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for amiodarone hydrochloride from Sun Pharmaceutical Industries, Inc., formally updating the approva…
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FDA approval · 2008-11-06FDA Approved: AMIODARONE HYDROCHLORIDE — Original Application (Advagen Pharma Limited)
FDA approved Amiodarone hydrochloride from Advagen Pharma Limited under an original application as a generic product. This indicates authori…
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FDA approval · 2008-09-16FDA Approved: AMIODARONE HYDROCHLORIDE — Original Application (Zydus Lifesciences Limited)
FDA approved AMIODARONE HYDROCHLORIDE from Zydus Lifesciences Limited under an original generic application.
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FDA approval · 2008-03-24FDA Approved: AMIODARONE HYDROCHLORIDE — Supplemental Application (Mylan Institutional LLC)
The FDA approved a supplemental application for amiodarone hydrochloride (generic antiarrhythmic) filed by Mylan Institutional LLC.
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FDA approval · 2008-02-25FDA Approved: AMIODARONE HYDROCHLORIDE — Original Application (Hikma Pharmaceuticals USA Inc.)
FDA approved Hikma Pharmaceuticals USA Inc. amiodarone hydrochloride generic (ANDA 077234), providing a generic option for the treatment of …
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FDA approval · 2007-11-16FDA Approved: PACERONE — Supplemental Application (Upsher-Smith Laboratories, LLC)
FDA approved a supplemental application for PACERONE (amiodarone hydrochloride) from Upsher-Smith Laboratories, LLC. The action modifies/exp…
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FDA approval · 2007-11-07FDA Approved: FLECAINIDE ACETATE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for flecainide acetate from Hikma Pharmaceuticals USA Inc., approving changes to the approved generi…