Urticaria
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Sign up freeTop drugs studied for this disease
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FDA approval · 2015-01-24FDA Approved: HYDROXYZINE PAMOATE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved Teva’s supplemental application for hydroxyzine pamoate, confirming its status as an approved generic drug. The action rela…
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FDA approval · 2015-01-24FDA Approved: HYDROXYZINE PAMOATE — Supplemental Application (Sandoz Inc)
The FDA approved a supplemental application for hydroxyzine pamoate submitted by Sandoz Inc (ANDA).
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FDA approval · 2015-01-20FDA Approved: ZYRTEC HIVES — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application expanding ZYRTEC HIVES (cetirizine hydrochloride) to include the treatment of hives/urticaria.
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FDA approval · 2014-12-30FDA Approved: CETIRIZINE HYDROCHLORIDE — Supplemental Application (Rising Pharma Holdings, Inc.)
The FDA approved a supplemental application for cetirizine hydrochloride by Rising Pharma Holdings, Inc., expanding regulatory approval for …
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CLINICAL_TRIALS research · 2014-12-16Clinical Trial Update: The Role of Vitamin D in Chronic Urticaria and Angioedema Treatment [NA]
A completed clinical trial investigating the role of vitamin D in treating chronic urticaria and angioedema, with results posted in 2014.
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FDA approval · 2014-12-02FDA Approved: ALLEGRA HIVES 24HR — Supplemental Application (Chattem, Inc.)
The FDA approved a supplemental application for Allegra Hives 24HR (fexofenadine hydrochloride) from Chattem, Inc., indicating a regulatory …
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FDA approval · 2014-11-07FDA Approved: HIVES RELIEF — Supplemental Application (WALGREEN COMPANY)
FDA approved a supplemental application for HIVES RELIEF, a cetirizine hydrochloride tablet product from Walgreens Company. The approval cov…
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FDA approval · 2014-11-05FDA Approved: HIVES RELIEF — Supplemental Application (WALGREEN COMPANY)
FDA approved a supplemental application for HIVES RELIEF, a cetirizine tablet product from Walgreens. Cetirizine is used to treat allergic s…
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CLINICAL_TRIALS trial_result · 2014-10-30Clinical Trial Update: An Efficacy and Safety Study of Desloratadine (MK-4117) in Japanese Participants With Chronic Urticaria (MK-4117-201) [Phase 3]
Phase 3 efficacy and safety results of desloratadine (MK-4117) in Japanese participants with chronic urticaria have been reported. The trial…
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FDA approval · 2014-09-26FDA Approved: ZYRTEC HIVES — Supplemental Application (Kenvue Brands LLC)
FDA approves a supplemental application for ZYRTEC HIVES (cetirizine hydrochloride) submitted by Kenvue Brands LLC. This action expands the …
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FDA approval · 2014-09-12FDA Approved: ALLEGRA HIVES 24HR — Supplemental Application (Chattem, Inc.)
The FDA approved a supplemental application for Allegra Hives 24HR (fexofenadine hydrochloride) submitted by Chattem, Inc., likely updating …
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CLINICAL_TRIALS trial_result · 2014-09-12Clinical Trial Update: Study to Investigate the Safety and Efficacy of Alesion® in Japanese Paediatric Patients With Urticaria
A completed clinical trial evaluated the safety and efficacy of Alesion in Japanese pediatric patients with urticaria.
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CLINICAL_TRIALS trial_result · 2014-09-12Clinical Trial Update: Post Marketing Surveillance of Alesion® in Japanese Paediatric Patients With Allergic Rhinitis, Eczema/Dermatitis, Urticaria and Pruritus
Post-marketing surveillance of Alesion in Japanese pediatric patients with allergic rhinitis, atopic dermatitis (eczema/dermatitis), urticar…
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FDA approval · 2014-08-19FDA Approved: GOOD NEIGHBOR PHARMACY CHILDRENS LORATADINE — Supplemental Application (AmerisourceBergen)
FDA approved a supplemental application for Good Neighbor Pharmacy Children's Loratadine (loratadine) from AmerisourceBergen. The approval i…
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FDA approval · 2014-07-22FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer HealthCare LLC)
FDA approved a supplemental NDA for Claritin RediTabs (loratadine) by Bayer HealthCare LLC.
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FDA approval · 2014-07-22FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer Healthcare LLC.)
FDA approved a supplemental application for Claritin RediTabs (loratadine) from Bayer Healthcare LLC, updating the approved formulation. Lor…
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CLINICAL_TRIALS trial_result · 2014-07-15Clinical Trial Update: Efficacy and Safety of Omalizumab in Patients With Severe Acute Urticaria [NA]
This clinical trial update evaluates the efficacy and safety of omalizumab for severe acute urticaria. The current status of the trial is UN…
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FDA approval · 2014-06-05FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for Hydroxyzine Hydrochloride from Teva Pharmaceuticals USA, Inc., granting regulatory clearance…
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FDA approval · 2014-06-04FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Amneal Pharmaceuticals LLC)
FDA approved Amneal Pharmaceuticals LLC's supplemental application for hydroxyzine hydrochloride, authorizing changes to the approved produc…
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FDA approval · 2014-06-03FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Northstar RxLLC)
FDA approved a supplemental application for hydroxyzine hydrochloride filed by Northstar RxLLC, enabling regulatory clearance related to the…
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FDA approval · 2014-06-03FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application for hydroxyzine hydrochloride (HYDROXYZINE HYDROCHLORIDE) from Chartwell RX, LLC.
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FDA approval · 2014-05-16FDA Approved: CHILDRENS ZYRTEC — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application for CHILDRENS ZYRTEC (cetirizine hydrochloride) submitted by Kenvue Brands LLC.
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FDA approval · 2014-05-15FDA Approved: CLARITIN ALLERGY — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Allergy (loratadine) by Bayer HealthCare LLC. The filing relates to labeling and/or ind…
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FDA approval · 2014-04-23FDA Approved: CLARINEX — Supplemental Application (Organon LLC)
The FDA approved a supplemental application for CLARINEX (desloratadine) from Organon LLC.
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FDA approval · 2014-04-16FDA Approved: ALLEGRA HIVES 24HR — Supplemental Application (Chattem, Inc.)
FDA approved a supplemental application for ALLEGRA HIVES 24HR (fexofenadine hydrochloride) from Chattem, Inc., authorizing an approved chan…