Atrial Fibrillation
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Sign up freeTop drugs studied for this disease
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FDA approval · 2007-03-01FDA Approved: SOTALOL HYDROCHLORIDE — Supplemental Application (Oxford Pharmaceuticals, LLC)
The FDA approved a supplemental application for Sotalol Hydrochloride (Oxford Pharmaceuticals, LLC), updating an existing approved product.
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FDA approval · 2007-02-08FDA Approved: DISOPYRAMIDE PHOSPHATE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for disopyramide phosphate from Teva Pharmaceuticals USA, Inc., indicating an approved update to…
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FDA approval · 2007-02-07FDA Approved: SOTALOL HYDROCHLORIDE — Original Application (Aurobindo Pharma Limited)
The FDA approved the original application for sotalol hydrochloride (generic) from Aurobindo Pharma Limited, authorizing its marketing as a …
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FDA approval · 2007-01-19FDA Approved: DIGOXIN — Supplemental Application (Amneal Pharmaceuticals NY LLC)
FDA approved a supplemental application for Digoxin (DIGOXIN) from Amneal Pharmaceuticals NY LLC.
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FDA approval · 2006-12-26FDA Approved: SOTALOL HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved Teva Pharmaceuticals USA, Inc.'s supplemental application for sotalol hydrochloride, a generic antiarrhythmic, under the AN…
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FDA approval · 2006-12-04FDA Approved: CARTIA XT — Supplemental Application (Actavis Pharma, Inc.)
FDA approved a supplemental application for CARTIA XT (diltiazem hydrochloride) submitted by Actavis Pharma, Inc., authorizing changes to th…
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FDA approval · 2006-07-05FDA Approved: WARFARIN SODIUM — Original Application (Teva Pharmaceuticals USA, Inc.)
FDA approves Teva's Warfarin Sodium generic under an Original Application (ANDA) for this oral anticoagulant.
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FDA approval · 2006-05-05FDA Approved: JANTOVEN — Supplemental Application (Upsher-Smith Laboratories, LLC)
FDA approved a supplemental application for JANTOVEN (warfarin sodium) from Upsher-Smith Laboratories, LLC.
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FDA approval · 2006-05-04FDA Approved: PROPAFENONE HYDROCHLORIDE — Supplemental Application (Strides Pharma Science Limited)
The FDA approved a supplemental application for Propafenone hydrochloride from Strides Pharma Science Limited, authorizing a generic Propafe…