Paroxysmal Supraventricular Tachycardia
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Sign up freeTop drugs studied for this disease
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FDA approval · 2022-03-17FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)
FDA approved the original Abbreviated New Drug Application for verapamil hydrochloride from Heritage Pharmaceuticals (d/b/a Avet) as a gener…
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CLINICAL_TRIALS trial_result · 2020-12-30Clinical Trial Update: Efficacy and Safety of Intranasal MSP-2017 (Etripamil) for the Conversion of PSVT to Sinus Rhythm [Phase 2]
Phase 2 trial evaluating intranasal MSP-2017 (etripamil) for converting paroxysmal supraventricular tachycardia to sinus rhythm; study compl…
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FDA approval · 2020-06-25FDA Approved: PROPAFENONE HYDROCHLORIDE — Original Application (Upsher-Smith Laboratories, LLC)
FDA approved Propafenone hydrochloride as an Original Application (generic) for Upsher-Smith Laboratories, LLC.
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FDA approval · 2020-04-29FDA Approved: DILTIAZEM HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved Teva's supplemental application for diltiazem hydrochloride (generic) under ANDA074185.
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FDA approval · 2020-03-27FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (Nivagen Pharmaceuticals, Inc.)
FDA approved a supplemental application for verapamil hydrochloride from Nivagen Pharmaceuticals, Inc., updating regulatory status for this …
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FDA approval · 2020-03-25FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Caplin Steriles Limited)
FDA approves Caplin Steriles Limited's Verapamil Hydrochloride under an Original Application (ANDA). This confirms the availability of a gen…
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FDA approval · 2019-11-14FDA Approved: PROPAFENONE HYDROCHLORIDE — Supplemental Application (Rising Pharma Holdings, Inc.)
The FDA approved a supplemental application for propafenone hydrochloride from Rising Pharma Holdings, providing a generic version of the an…
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FDA approval · 2019-10-31FDA Approved: PROPAFENONE HYDROCHLORIDE — Supplemental Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved a supplemental application for Propafenone Hydrochloride from Glenmark Pharmaceuticals Inc., USA.
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FDA approval · 2019-10-30FDA Approved: PROPAFENONE HYDROCHLORIDE — Supplemental Application (ANI Pharmaceuticals, Inc.)
The FDA approved ANI Pharmaceuticals' supplemental application for propafenone hydrochloride, a generic antiarrhythmic drug. This approval s…
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FDA approval · 2019-10-01FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals Inc)
The FDA approved a supplemental application for Verapamil Hydrochloride by Teva Pharmaceuticals Inc., updating the drug’s labeling and appro…
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FDA approval · 2019-09-25FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (Nivagen Pharmaceuticals, Inc.)
The FDA approved a supplemental application for verapamil hydrochloride (generic) from Nivagen Pharmaceuticals, Inc., authorizing the sale o…
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FDA approval · 2019-01-04FDA Approved: PROPAFENONE HYDROCHLORIDE — Original Application (Vitruvias Therapeutics)
FDA approved Propafenone hydrochloride as an Abbreviated New Drug Application (ANDA) for a generic antiarrhythmic, with Vitruvias Therapeuti…
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FDA approval · 2018-06-18FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Somerset Therapeutics, LLC)
The FDA approved the original application for Verapamil Hydrochloride by Somerset Therapeutics, LLC, enabling a generic version of verapamil…
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FDA approval · 2018-06-18FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Somerset Therapeutics, LLC)
FDA approves Somerset Therapeutics' Verapamil hydrochloride as an original application, granting a generic version of the drug.
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FDA approval · 2018-04-16FDA Approved: ADENOSINE — Original Application (Fresenius Kabi USA, LLC)
FDA approves the original application for adenosine from Fresenius Kabi USA, LLC (generic adenosine) under ANDA205568.
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FDA approval · 2018-02-16FDA Approved: ADENOSINE — Original Application (Sagent Pharmaceuticals)
FDA approved the original application for Adenosine from Sagent Pharmaceuticals, establishing a generic intravenous form for treating paroxy…
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FDA approval · 2017-12-13FDA Approved: DILTIAZEM HYDROCHLORIDE — Supplemental Application (Hospira, Inc.)
FDA approved a supplemental application for diltiazem hydrochloride filed by Hospira, Inc., signaling an additional approval related to the …
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FDA approval · 2017-11-27FDA Approved: ADENOSINE — Original Application (Fresenius Kabi USA, LLC)
FDA approved the original application for Adenosine from Fresenius Kabi USA, LLC for injection. The product is used to interrupt paroxysmal …
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FDA approval · 2017-11-17FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application for verapamil hydrochloride from Chartwell RX, LLC.
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FDA approval · 2017-11-02FDA Approved: ADENOSINE — Original Application (Eugia US LLC)
FDA approves a generic adenosine product under Original Application (ANDA205331) by Eugia US LLC.
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FDA approval · 2017-05-05FDA Approved: VERAPAMIL HYDROCHLORIDE — Original Application (Nivagen Pharmaceuticals, Inc.)
The FDA approved the original application for verapamil hydrochloride from Nivagen Pharmaceuticals, Inc. as a generic product.
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FDA approval · 2016-11-18FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (Wilshire Pharmaceuticals, Inc.)
FDA approved a supplemental application for verapamil hydrochloride from Wilshire Pharmaceuticals, Inc., updating the existing NDA.
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FDA label_change · 2016-11-18FDA Approved: CARDIZEM LA — Supplemental Application (Bausch Health US LLC)
FDA approved a supplemental application for Cardizem LA (diltiazem hydrochloride extended-release) submitted by Bausch Health US LLC.
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FDA approval · 2016-11-18FDA Approved: VERAPAMIL HYDROCHLORIDE — Supplemental Application (EXELA PHARMA SCIENCES, LLC)
The FDA approved a supplemental application for verapamil hydrochloride from Exela Pharma Sciences, LLC.
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FDA approval · 2016-05-11FDA Approved: PROPAFENONE HYDROCHLORIDE — Original Application (Aurobindo Pharma Limited)
FDA approved the original application for propafenone hydrochloride (generic) manufactured by Aurobindo Pharma Limited.