Urticaria
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Sign up freeTop drugs studied for this disease
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FDA approval · 2022-07-08FDA Approved: ALLERGY RELIEF — Supplemental Application (Publix Super Markets Inc)
FDA approved a supplemental application for Allergy Relief containing fexofenadine hydrochloride, submitted by Publix Super Markets Inc.
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EMA approval · 2022-06-24EMA Authorised: Desloratadine ratiopharm (desloratadine) — Ratiopharm GmbH
Authorised desloratadine product Desloratadine ratiopharm by Ratiopharm GmbH for allergic rhinitis and urticaria indications.
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EMA approval · 2022-06-09EMA Authorised: Dasselta (desloratadine) — Krka, d.d., Novo mesto
Dasselta (desloratadine) by Krka has been authorised for allergic rhinitis (perennial and seasonal) and urticaria in the EU.
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FDA approval · 2021-12-14FDA Approved: ZYRTEC — Supplemental Application (Kenvue Brands LLC)
FDA approves a supplemental application for ZYRTEC (cetirizine hydrochloride) submitted by Kenvue Brands LLC.
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FDA approval · 2021-10-13FDA Approved: ALLEGRA HIVES 24HR — Supplemental Application (Chattem, Inc.)
The FDA approved a supplemental application for Allegra Hives 24HR, a fexofenadine hydrochloride product from Chattem, expanding its labelin…
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FDA approval · 2021-07-12FDA Approved: PROMETHAZINE HYDROCHLORIDE — Original Application (QUAGEN PHARMACEUTICALS LLC)
FDA approved promethazine hydrochloride under an original ANDA for Quagen Pharmaceuticals LLC.
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FDA approval · 2021-04-02FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application to add a chewable grape and bubblegum formulation of loratadine (Claritin) by Bayer HealthCare LLC.
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FDA approval · 2021-03-25FDA Approved: CARBINOXAMINE MALEATE EXTENDED-RELEASE ORAL SUSPENSION — Supplemental Application (Neos Therapeutics, LP)
FDA approved a supplemental application to authorize an extended-release oral suspension formulation of carbinoxamine maleate, submitted by …
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FDA approval · 2021-01-11FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer Healthcare LLC.)
FDA approved a supplemental application for CLARITIN REDITABS (loratadine) from Bayer Healthcare LLC., enabling a new or revised indication …
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FDA approval · 2021-01-07FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
The FDA approved a supplemental application for Claritin Chewable Grape and Bubblegum (loratadine) by Bayer HealthCare LLC, adding a chewabl…
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FDA approval · 2020-12-07FDA Approved: CETIRIZINE HCL — Supplemental Application (AMERISOURCE BERGEN)
The FDA approved a supplemental application for cetirizine hydrochloride submitted by AmerisourceBergen.
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FDA approval · 2020-10-30FDA Approved: LORATADINE — Original Application (Tenshi Kaizen Pvt Ltd)
FDA approved an original generic application for loratadine (Tenshi Kaizen Pvt Ltd).
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FDA approval · 2020-09-21FDA Approved: ALL DAY ALLERGY — Original Application (WALMART INC. (see also Equate))
FDA approved Walmart's All Day Allergy cetirizine hydrochloride as an original generic application (ANDA 213105), enabling a Walmart/Equate …
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FDA approval · 2020-09-18FDA Approved: LORATADINE — Original Application (Tenshi Kaizen Pvt Ltd)
FDA approved Tenshi Kaizen Pvt Ltd's Loratadine as an original generic application. The product is indicated for allergic rhinitis and urtic…
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FDA approval · 2020-09-11FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Aurohealth LLC)
FDA approved the original generic application for cetirizine hydrochloride to be marketed by Aurohealth LLC.
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FDA approval · 2020-08-07FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application to add Claritin Chewable Grape and Bubblegum (loratadine) as a new chewable dosage form. This expand…
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FDA approval · 2020-03-17FDA Approved: DIPHENHYDRAMINE HYDROCHLORIDE — Supplemental Application (PAI Holdings, LLC dba PAI Pharma)
FDA approved a supplemental application for Diphenhydramine hydrochloride from PAI Pharma, indicating an approved modification to an existin…
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FDA approval · 2020-03-03FDA Approved: ALLERGY RELIEF — Supplemental Application (Ohm Laboratories Inc.)
FDA approved a supplemental application for Allergy Relief (loratadine) from Ohm Laboratories Inc.
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FDA approval · 2020-03-03FDA Approved: CETIRIZINE HYDROCHLORIDE — Supplemental Application (Padagis Israel Pharmaceuticals Ltd)
FDA approved a supplemental application for cetirizine hydrochloride from Padagis Israel Pharmaceuticals Ltd. It is a generic antihistamine …
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FDA approval · 2020-03-03FDA Approved: CETIRIZINE HYDROCHLORIDE — Supplemental Application (Bionpharma Inc.)
The FDA approved a supplemental application for cetirizine hydrochloride by Bionpharma Inc., under ANDA078488, granting regulatory approval …
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FDA approval · 2020-02-24FDA Approved: ALLERGY RELIEF — Original Application (Publix Super Markets Inc)
FDA approved Publix Super Markets Inc's original application for a generic fexofenadine hydrochloride allergy relief product (brand name All…
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FDA approval · 2019-12-31FDA Approved: GOOD SENSE LEVOCETIRIZINE — Supplemental Application (L. Perrigo Company)
FDA approved a supplemental application for Good Sense Levocetirizine (levocetirizine dihydrochloride) from L. Perrigo Company.
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FDA approval · 2019-12-13FDA Approved: CETIRIZINE HCL — Supplemental Application (AMERISOURCE BERGEN)
FDA approved a supplemental application for Cetirizine HCl submitted by AmerisourceBergen, updating the NDA to reflect the approved suppleme…
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FDA approval · 2019-11-07FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
The FDA approved a supplemental application to add a chewable grape and bubblegum formulation of Claritin (loratadine) from Bayer HealthCare…
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FDA approval · 2019-10-25FDA Approved: ALLERGY RELIEF 24HR — Supplemental Application (VELOCITY PHARMA LLC)
FDA approved a supplemental application for ALLERGY RELIEF 24HR (levocetirizine dihydrochloride) by Velocity Pharma LLC.