Urticaria
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Sign up freeTop drugs studied for this disease
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FDA approval · 2010-01-21FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals LLC)
The FDA approved Amneal Pharmaceuticals' original application for cetirizine hydrochloride, granting a generic version of cetirizine for all…
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FDA approval · 2009-11-12FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Rising Pharma Holdings, Inc.)
FDA approved cetirizine hydrochloride under an original application for use as a generic antihistamine indicated for allergic rhinitis and u…
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FDA approval · 2009-10-07FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals LLC)
FDA approved a generic cetirizine hydrochloride product under an Original Abbreviated New Drug Application by Amneal Pharmaceuticals LLC.
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FDA approval · 2009-08-31FDA Approved: GOOD NEIGHBOR PHARMACY CHILDRENS LORATADINE — Supplemental Application (AmerisourceBergen)
The FDA approved a supplemental application for Good Neighbor Pharmacy Children's Loratadine (loratadine) submitted by AmerisourceBergen.
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FDA approval · 2009-08-26FDA Approved: ALLERGY RELIEF — Original Application (Prodose, Inc)
FDA approved an original application for ALLERGY RELIEF containing cetirizine hydrochloride, marketed by Prodose, Inc.
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FDA approval · 2009-06-10FDA Approved: DIPHENHYDRAMINE HYDROCHLORIDE — Supplemental Application (PAI Holdings, LLC dba PAI Pharma)
FDA approved a supplemental application for diphenhydramine hydrochloride (PAI Pharma) under an ANDA.
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FDA approval · 2009-05-28FDA Approved: ALLERGY RELIEF CHILDRENS — Supplemental Application (CVS Pharmacy)
FDA approved a supplemental application for ALLERGY RELIEF CHILDRENS containing cetirizine hydrochloride by CVS Pharmacy.
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FDA approval · 2009-05-28FDA Approved: CHILDRENS CETIRIZINE HYDROCHLORIDE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
FDA approved a supplemental application for Children's Cetirizine Hydrochloride from Sun Pharmaceutical Industries, Inc., under an ANDA subm…
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FDA approval · 2009-04-06FDA Approved: CLARITIN LIQUI-GELS — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Liqui-Gels (loratadine) submitted by Bayer HealthCare LLC, pertaining to this formulati…
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FDA approval · 2009-03-30FDA Approved: CETRIZINE HYDROCHLORIDE — Original Application (APOZEAL PHARMACEUTICALS INC)
FDA approved cetirizine hydrochloride from APOZEAL Pharmaceuticals Inc as an original application; a generic antihistamine indicated for all…
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FDA approval · 2009-03-24FDA Approved: LORATADINE ALLERGY RELIEF — Supplemental Application (DISCOUNT DRUG MART)
FDA approved a supplemental application for Loratadine Allergy Relief from Discount Drug Mart.
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FDA approval · 2009-03-19FDA Approved: CAREONE ALLERGY RELIEF — Supplemental Application (American Sales Company)
FDA's entry documents a supplemental application for CAREONE ALLERGY RELIEF (fexofenadine HCl) submitted by American Sales Company.
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FDA approval · 2009-03-13FDA Approved: CHILDRENS ZYRTEC — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for Children's Zyrtec (cetirizine hydrochloride) filed by Kenvue Brands LLC.
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FDA approval · 2009-02-19FDA Approved: HIVES RELIEF — Original Application (WALGREEN COMPANY)
FDA approved Walgreen's HIVES RELIEF as an original ANDA for cetirizine tablets (cetirizine hydrochloride). This provides a generic option f…
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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 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 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.