Urticaria
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Sign up freeTop drugs studied for this disease
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FDA approval · 2017-12-22FDA Approved: CURIST ALLERGY RELIEF — Original Application (Little Pharma, Inc.)
FDA approves CURIST ALLERGY RELIEF through an original ANDA for cetirizine hydrochloride, authorizing the generic for allergy symptom relief…
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FDA approval · 2017-12-08FDA Approved: ZYRTEC HIVES — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for ZYRTEC HIVES (cetirizine hydrochloride) by Kenvue Brands LLC. The approval confirms the ceti…
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FDA approval · 2017-11-09FDA Approved: CHILDRENS FEXOFENADINE HYDROCHLORIDE ALLERGY — Original Application (Wal-Mart Stores Inc)
FDA approved a generic version of fexofenadine hydrochloride for pediatric allergy uses under an Original Application with Wal-Mart Stores I…
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FDA approval · 2017-08-31FDA Approved: LEVOCETIRIZINE DIHYDROCHLORIDE — Supplemental Application (Marlex Pharmaceuticals Inc)
FDA approved a supplemental application for levocetirizine dihydrochloride from Marlex Pharmaceuticals, updating an existing approved produc…
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FDA approval · 2017-07-21FDA Approved: ALLERGY RELIEF — Original Application (WALMART INC. (see also Equate))
FDA approved Walmart's ALLERGY RELIEF containing cetirizine hydrochloride as an original generic application (ANDA 205291) for allergy relie…
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FDA approval · 2017-07-10FDA Approved: ALLERGY RELIEF CHILDRENS — Supplemental Application (CVS Pharmacy)
FDA approved a supplemental application for CVS Pharmacy's ALLERGY RELIEF CHILDRENS cetirizine hydrochloride product.
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FDA approval · 2017-05-22FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Chewable Grape and Bubblegum (loratadine) from Bayer HealthCare LLC. The approval expan…
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FDA approval · 2017-05-19FDA Approved: CYPROHEPTADINE HYDROCHLORIDE — Original Application (Zydus Pharmaceuticals USA Inc.)
FDA approved a generic cyproheptadine hydrochloride product from Zydus Pharmaceuticals USA Inc (ANDA 208938). Indications include relief of …
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FDA approval · 2017-05-16FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer Healthcare LLC.)
FDA approved a supplemental application for Claritin RediTabs (loratadine) from Bayer Healthcare LLC. Claritin RediTabs is an antihistamine …
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FDA approval · 2016-11-08FDA Approved: CETIRIZINE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for cetirizine hydrochloride from Sun Pharmaceutical Industries, Inc., under the existing ANDA.
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FDA approval · 2016-11-08FDA Approved: CETIRIZINE HYDROCHLORIDE — Supplemental Application (Padagis Israel Pharmaceuticals Ltd)
FDA approved a supplemental application for cetirizine hydrochloride by Padagis Israel Pharmaceuticals Ltd. The document indicates the actio…
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FDA approval · 2016-11-08FDA Approved: CETIRIZINE HYDROCHLORIDE — Supplemental Application (Bionpharma Inc.)
FDA approves a supplemental application for cetirizine hydrochloride from Bionpharma Inc. This represents approval of a supplemental NDA for…
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FDA approval · 2016-11-08FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Chartwell RX, LLC)
FDA approved a supplemental application for hydroxyzine hydrochloride (Chartwell RX, LLC), resulting in a labeling update for this generic p…
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FDA approval · 2016-11-08FDA Approved: CETIRIZINE HYDROCHLORIDE ORAL SOLUTION — Supplemental Application (APOZEAL PHARMACEUTICALS INC)
FDA approved a supplemental application for Cetirizine Hydrochloride Oral Solution from APOZEAL Pharmaceuticals Inc.
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FDA approval · 2016-11-08FDA Approved: CETIRIZINE HYDROCHLORIDE — Supplemental Application (Rising Pharma Holdings, Inc.)
The FDA approved a supplemental application for cetirizine hydrochloride submitted by Rising Pharma Holdings, Inc. under an ANDA.
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FDA approval · 2016-11-04FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer Healthcare LLC.)
The FDA approved a supplemental application for Claritin RediTabs (loratadine) submitted by Bayer Healthcare LLC, under the existing NDA.
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FDA approval · 2016-08-12FDA Approved: CAREONE ALLERGY RELIEF — Original Application (American Sales Company)
FDA approved CAREONE ALLERGY RELIEF as an original application for cetirizine hydrochloride tablets (generic antihistamine) from American Sa…
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FDA approval · 2016-08-09FDA Approved: CLARITIN ALLERGY — Supplemental Application (Bayer HealthCare LLC.)
The FDA approved a supplemental application for Claritin Allergy (loratadine) from Bayer HealthCare LLC.
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FDA approval · 2016-08-05FDA Approved: CHILDRENS ALLEGRA ALLERGY — Supplemental Application (Chattem, Inc.)
The FDA approved a supplemental application for Children's Allegra Allergy (fexofenadine hydrochloride) to modify the labeling related to pe…
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FDA approval · 2016-06-10FDA Approved: CHILDRENS ALLEGRA ALLERGY — Supplemental Application (Chattem, Inc.)
FDA approved a supplemental application for Children's Allegra Allergy (fexofenadine hydrochloride) from Chattem, Inc., marking an additiona…
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FDA approval · 2016-05-31FDA Approved: RYVENT — Original Application (Carwin Pharmaceutical Associates, LLC)
FDA approved Ryvent (carbinoxamine maleate) in relation to its original application for this generic antihistamine from Carwin Pharmaceutica…
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FDA approval · 2016-05-12FDA Approved: CARBINOXAMINE MALEATE EXTENDED-RELEASE ORAL SUSPENSION — Supplemental Application (Neos Therapeutics, LP)
FDA approved a supplemental application to authorize a new extended-release oral suspension formulation of carbinoxamine maleate by Neos The…
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FDA approval · 2016-04-05FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
The FDA approved a supplemental application to add grape and bubblegum chewable forms of Claritin (loratadine) from Bayer HealthCare LLC, ex…
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FDA approval · 2016-04-04FDA Approved: ZYRTEC HIVES — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental application for ZYRTEC HIVES (cetirizine hydrochloride) to treat hives (urticaria). The product is manufactured …
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FDA approval · 2016-03-30FDA Approved: HYDROXYZINE HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for hydroxyzine hydrochloride by Teva Pharmaceuticals USA, Inc., under ANDA088617.