Allergic Rhinitis
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Sign up freeTop drugs studied for this disease
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FDA approval · 2009-04-30FDA Approved: AZELASTINE HYDROCHLORIDE — Original Application (Apotex Corp.)
FDA approved Apotex Corp.'s original application for azelastine hydrochloride, a generic antihistamine product.
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FDA approval · 2009-04-27FDA Approved: CETIRIZINE HYDROCHLORIDE ORAL SOLUTION — Original Application (APOZEAL PHARMACEUTICALS INC)
FDA approved Apozeal Pharmaceuticals' cetirizine hydrochloride oral solution as an original generic product.
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FDA approval · 2009-04-23FDA Approved: CLARITIN-D 12 HOUR — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin-D 12 Hour, a loratadine and pseudoephedrine sulfate combination product from Bayer Heal…
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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 · 2009-03-27FDA Approved: ALLERGY CONGESTION RELIEF — Supplemental Application (Kroger Company)
FDA approved Kroger's supplemental application for Allergy Congestion Relief, a product combining loratadine and pseudoephedrine sulfate. It…
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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 · 2009-03-20FDA Approved: COUNTERACT ALLERGY — Supplemental Application (Melaleuca, Inc.)
FDA approved a supplemental application for COUNTERACT ALLERGY (loratadine) from Melaleuca, Inc. This approval confirms the product as an ap…
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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 · 2009-01-29FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer Healthcare LLC.)
FDA approved a supplemental application for Claritin RediTabs (loratadine) from Bayer Healthcare LLC.
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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 · 2008-10-06FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (Bionpharma Inc.)
FDA approved Bionpharma Inc.'s original application for cetirizine hydrochloride, a generic antihistamine for allergic rhinitis and chronic …
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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 · 2008-07-25FDA Approved: CLARITIN ALLERGY — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Allergy (loratadine) from Bayer HealthCare LLC to update the labeling.
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FDA approval · 2008-07-21FDA Approved: FLUTICASONE PROPIONATE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved Hikma Pharmaceuticals USA Inc.'s supplemental application for Fluticasone Propionate, approving an updated or additional ge…
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FDA approval · 2008-07-01FDA Approved: FLUTICASONE PROPIONATE HFA — Supplemental Application (Prasco Laboratories)
FDA approved a supplemental application for Fluticasone Propionate HFA submitted by Prasco Laboratories.
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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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FDA approval · 2008-04-24FDA Approved: SINGULAIR — Supplemental Application (Organon LLC)
The FDA approved a supplemental application for Singulair (montelukast sodium) by Organon LLC, updating the product indication/label as part…
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FDA approval · 2008-04-24FDA Approved: PROMETHAZINE HYDROCHLORIDE — Original Application (XGen Pharmaceuticals DJB, Inc.)
The FDA approved the original ANDA for Promethazine hydrochloride (Promethazine HCl) from XGen Pharmaceuticals DJB, Inc. The approval covers…