Urticaria
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Sign up freeTop drugs studied for this disease
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FDA label_change · 2008-11-25FDA Approved: ZYRTEC HIVES — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application for ZYRTEC HIVES, updating its labeling to reflect cetirizine hydrochloride for the treatment of urt…
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FDA approval · 2008-10-21FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer HealthCare LLC)
FDA approved a supplemental application for Claritin RediTabs (loratadine) from Bayer HealthCare LLC. This action approves the loratadine Re…
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FDA approval · 2008-10-21FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer Healthcare LLC.)
FDA approves a supplemental application for Claritin RediTabs (loratadine) from Bayer Healthcare LLC.
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FDA label_change · 2008-10-21FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a labeling supplement for Claritin Chewable Grape and Bubblegum (loratadine) by Bayer HealthCare LLC.
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FDA label_change · 2008-10-08FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
FDA supplemental application approval for Claritin Chewable Grape and Bubblegum (loratadine) to add a new chewable flavor formulation, updat…
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FDA approval · 2008-09-24FDA Approved: HYDROXYZINE HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals LLC)
The FDA approved Amneal Pharmaceuticals LLC's hydroxyzine hydrochloride as a generic drug under ANDA 040808.
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FDA approval · 2008-08-14FDA Approved: CHILDRENS ZYRTEC — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for Children's Zyrtec (cetirizine hydrochloride) submitted by Kenvue Brands LLC, updating the pr…
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FDA approval · 2008-08-05FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for hydroxyzine hydrochloride from Teva Pharmaceuticals USA, Inc., confirming continued approval of …
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FDA label_change · 2008-08-05FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for Hydroxyzine Hydrochloride (Teva Pharmaceuticals USA, Inc.), updating the labeling.
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FDA approval · 2008-06-25FDA Approved: ALLEGRA HIVES 24HR — Supplemental Application (Chattem, Inc.)
FDA approved a supplemental application for Allegra Hives 24HR (fexofenadine hydrochloride) submitted by Chattem, Inc.
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FDA approval · 2008-06-20FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical's cetirizine hydrochloride under an original generic application, enabling a generic cetirizine hydrochlorid…
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FDA approval · 2008-06-18FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (PAI Holdings, LLC dba PAI Pharma)
FDA approves the original application for cetirizine hydrochloride as a generic drug to be marketed by PAI Holdings, dba PAI Pharma.
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FDA approval · 2008-06-17FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Padagis Israel Pharmaceuticals Ltd)
The FDA approved Padagis Israel Pharmaceuticals Ltd's original application for a generic cetirizine hydrochloride product.
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FDA approval · 2008-06-16FDA Approved: CLARITIN LIQUI-GELS — Original Application (Bayer HealthCare LLC.)
The FDA approved CLARITIN LIQUI-GELS (loratadine) under an Original Application from Bayer HealthCare LLC, adding a liquid-filled gel capsul…
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FDA approval · 2008-05-29FDA Approved: HYDROXYZINE HYDROCHLORIDE — Original Application (Camber Pharmaceuticals, Inc.)
FDA approved Camber Pharmaceuticals' hydroxyzine hydrochloride under an original ANDA; generic entry approved for its existing indications.
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CLINICAL_TRIALS trial_result · 2008-05-07Clinical Trial Update: Effect of Anti-IgE in Chronic Urticaria [Phase 2]
Phase 2 trial evaluating anti-IgE therapy for chronic urticaria has completed.
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FDA approval · 2008-04-22FDA Approved: CHILDRENS CETIRIZINE HYDROCHLORIDE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved the original application for Sun Pharmaceutical's Children's cetirizine hydrochloride, a generic cetirizine product for pediatr…
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FDA approval · 2008-04-09FDA Approved: ALLERGY RELIEF CHILDRENS — Original Application (CVS Pharmacy)
FDA approved a pediatric cetirizine hydrochloride product under an original application for Allergy Relief Childrens (CVS Pharmacy).
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FDA approval · 2008-03-31FDA Approved: HYDROXYZINE HYDROCHLORIDE — Original Application (Northstar RxLLC)
FDA approved Northstar RxLLC's Original Application for hydroxyzine hydrochloride, a generic antihistamine product.
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CLINICAL_TRIALS trial_result · 2008-03-04Clinical Trial Update: Induction of Suction Blisters in Patients With Urticaria, Blistering Diseases, Inflammatory Dermatoses and Neoplastic Disorders, and in Normal Volunteers
A status update on a clinical trial investigating suction blister induction in participants including those with dermatitis, urticaria, vesi…
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FDA approval · 2008-03-03FDA Approved: GOOD NEIGHBOR PHARMACY CHILDRENS LORATADINE — Supplemental Application (AmerisourceBergen)
FDA approved a supplemental application for Good Neighbor Pharmacy Children's Loratadine (loratadine) from AmerisourceBergen, indicating app…
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FDA approval · 2008-02-14FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Sandoz Inc)
FDA approved the original application for cetirizine hydrochloride from Sandoz Inc., a generic antihistamine used to treat allergic rhinitis…
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FDA approval · 2007-12-31FDA Approved: CAREONE ALLERGY RELIEF — Supplemental Application (American Sales Company)
FDA approved a supplemental application for CAREONE ALLERGY RELIEF (fexofenadine hydrochloride) under ANDA076447, filed by American Sales Co…
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FDA approval · 2007-12-28FDA Approved: CETIRIZINE HCL — Original Application (GLENMARK THERAPEUTICS INC., USA)
FDA approved Glenmark's cetirizine HCl Original Application (ANDA), granting marketing rights for a generic cetirizine product. Indications …
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FDA approval · 2007-12-27FDA Approved: ALL DAY ALLERGY RELIEF — Original Application (Dolgencorp, Inc. (DOLLAR GENERAL & REXALL))
FDA approved ALL DAY ALLERGY RELIEF (cetirizine hydrochloride) from Dolgencorp as an original application for an over-the-counter antihistam…