Herpes Simplex Virus Infections
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Sign up freeTop drugs studied for this disease
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CLINICAL_TRIALS trial_result · 2026-01-05Clinical Trial Update: Efficacy and Safety of Acyclovir-penciclovir Cream Versus an Abreva in the Suppression of Herpes Simplex Virus Eruptions [Phase 2]
A Phase 2 trial comparing acyclovir-penciclovir cream to Abreva for suppression of herpes simplex eruptions has completed, reporting efficac…
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FDA approval · 2023-11-29FDA Approved: FOSCARNET SODIUM — Original Application (Hikma Pharmaceuticals USA Inc.)
FDA approved the original application for Foscarnet Sodium, a generic antiviral intended for CMV and acyclovir-resistant HSV infections.
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FDA approval · 2021-11-01FDA Approved: ACYCLOVIR — Supplemental Application (Amneal Pharmaceuticals LLC)
The FDA approved Amneal Pharmaceuticals LLC's supplemental application for acyclovir.
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FDA approval · 2020-12-23FDA Approved: ACYCLOVIR — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for acyclovir submitted by Teva Pharmaceuticals USA, Inc.
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FDA approval · 2020-07-10FDA Approved: ACYCLOVIR — Original Application (ANI Pharmaceuticals, Inc.)
FDA approved ANI Pharmaceuticals' original ANDA for generic acyclovir (acyclovir). The approval covers treatment of herpes simplex infection…
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FDA approval · 2020-02-28FDA Approved: VALACYCLOVIR — Supplemental Application (SUN PHARMACEUTICAL INDUSTRIES, INC.)
The FDA approved a supplemental application for valacyclovir from Sun Pharmaceutical Industries, Inc., resulting in changes to the product's…
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FDA approval · 2019-07-25FDA Approved: FAMCICLOVIR — Supplemental Application (Macleods Pharmaceuticals Limited)
The FDA approved a supplemental application for famciclovir from Macleods Pharmaceuticals Limited under an ANDA.
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FDA approval · 2019-03-15FDA Approved: ACYCLOVIR — Original Application (Viona Pharmaceuticals Inc)
FDA approved the generic acyclovir product from Viona Pharmaceuticals Inc under an Original Application.
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FDA approval · 2017-08-16FDA Approved: ACYCLOVIR — Original Application (Carlsbad Technology, Inc.)
FDA approves a generic acyclovir product under an Original Application (ANDA) from Carlsbad Technology, Inc.
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FDA approval · 2017-07-31FDA Approved: ACYCLOVIR — Original Application (Northstar Rx LLC)
FDA approved Northstar Rx LLC's acyclovir as a generic under an original ANDA, authorizing its sale as a generic acyclovir product. The appr…
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FDA approval · 2016-11-10FDA Approved: FOSCAVIR — Supplemental Application (Clinigen Limited)
The FDA approved a supplemental application for FOSCAVIR (foscarnet sodium) submitted by Clinigen Limited.
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FDA approval · 2016-04-08FDA Approved: ACYCLOVIR — Supplemental Application (Quinn Pharmaceuticals)
FDA approved a supplemental application for acyclovir submitted by Quinn Pharmaceuticals, indicating regulatory approval of a supplement for…
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FDA approval · 2014-04-01FDA Approved: ACYCLOVIR — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for acyclovir from Teva Pharmaceuticals USA, Inc., updating the drug’s approval details. The supplem…
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FDA approval · 2014-03-06FDA Approved: ACYCLOVIR — Original Application (Nivagen Pharmaceuticals, Inc.)
FDA approved the original ANDA for acyclovir from Nivagen Pharmaceuticals, authorizing a generic version of the antiviral for several herpes…
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FDA approval · 2013-11-15FDA Approved: ACYCLOVIR — Original Application (Modavar Pharmaceuticals LLC)
FDA approved Modavar Pharmaceuticals LLC's original ANDA for acyclovir, enabling a generic version of the antiviral for common herpes simple…
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FDA approval · 2013-05-14FDA Approved: VALACYCLOVIR — Supplemental Application (SUN PHARMACEUTICAL INDUSTRIES, INC.)
FDA approved a supplemental application for VALACYCLOVIR from Sun Pharmaceutical Industries, Inc., under an approved ANDA.
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FDA approval · 2013-03-20FDA Approved: VALACYCLOVIR HYDROCHLORIDE — Supplemental Application (TIME CAP LABORATORIES, INC.)
FDA approved a supplemental application for valacyclovir hydrochloride from Time Cap Laboratories, Inc. The action finalizes the regulatory …
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FDA approval · 2013-03-15FDA Approved: VALACYCLOVIR HYDROCHLORIDE — Supplemental Application (Aurobindo Pharma Limited)
The FDA approved a supplemental application for Valacyclovir hydrochloride from Aurobindo Pharma Limited. This action supports the continued…
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CLINICAL_TRIALS trial_result · 2012-06-11Clinical Trial Update: A Randomized Double-Blind Control-Comparison Crossover Trial of Oral Glutamine to Suppress Frequently Recurrent Herpes Labialis [Phase 2]
Phase 2 randomized, double-blind, crossover trial evaluating oral glutamine to suppress frequently recurrent herpes labialis; the study was …
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FDA approval · 2011-03-21FDA Approved: FAMCICLOVIR — Original Application (Aurobindo Pharma Limited)
The FDA approved Aurobindo Pharma Limited's generic famciclovir under an Original Application (ANDA), authorizing its sale in the United Sta…
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FDA approval · 2010-05-24FDA Approved: VALACYCLOVIR HYDROCHLORIDE — Original Application (TIME CAP LABORATORIES, INC.)
FDA approved Valacyclovir hydrochloride from Time Cap Laboratories under an Original Abbreviated New Drug Application.