Urticaria
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Sign up freeTop drugs studied for this disease
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FDA label_change · 2019-06-17FDA 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.
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FDA approval · 2019-06-12FDA Approved: CHILDRENS ALLERGY RELIEF — Original Application (H E B)
FDA approved an original ANDA for Children's Allergy Relief containing loratadine, a generic antihistamine manufactured by H E B.
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FDA approval · 2019-05-22FDA Approved: CYPROHEPTADINE HYDROCHLORIDE — Original Application (QUAGEN PHARMACEUTICALS LLC)
FDA approved Cyproheptadine hydrochloride from Quagen Pharmaceuticals LLC under an Original Application for a generic product.
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FDA approval · 2019-05-16FDA Approved: CETIRIZINE HYDROCHLORIDE — Original Application (QUAGEN PHARMACEUTICALS LLC)
FDA approved cetirizine hydrochloride under an original ANDA for QUAGEN PHARMACEUTICALS LLC as an oral antihistamine indicated for relief of…
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FDA approval · 2019-04-01FDA Approved: LEVOCETIRIZINE DIHYDROCHLORIDE — Original Application (Camber Pharmaceuticals, Inc.)
The FDA approved Camber Pharmaceuticals' original application for a generic levocetirizine dihydrochloride product, an antihistamine indicat…
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FDA approval · 2019-03-13FDA Approved: CHILDRENS ALLERGY RELIEF — Original Application (Strategic Sourcing Services)
FDA approves an Original ANDA for Cetirizine Hydrochloride marketed as Children's Allergy Relief from Strategic Sourcing Services.
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FDA label_change · 2019-02-28FDA Approved: CLARITIN ALLERGY — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Allergy (loratadine) by Bayer HealthCare LLC, indicating a labeling change or addition.…
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CLINICAL_TRIALS trial_result · 2019-02-18Clinical Trial Update: Real-life Management and Therapeutic Outcome of Patients With Chronic Rhinitis and Chronic Urticaria in Thailand
A completed clinical trial from Thailand reports real-world management and therapeutic outcomes for patients with allergic rhinitis, nonalle…
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CLINICAL_TRIALS research · 2019-02-08Clinical Trial Update: The Validity, Reliability and Interpretability of Thai-version of Chronic Urticaria Quality of Life Questionnaire
A completed Mahidol University study validating the Thai version of the Chronic Urticaria Quality of Life Questionnaire, assessing validity,…
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FDA label_change · 2019-02-06FDA Approved: CLARITIN — Supplemental Application (Bayer HealthCare LLC)
FDA approved a supplemental application for Claritin (loratadine) submitted by Bayer HealthCare LLC. The action involves updates to the prod…
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FDA approval · 2019-01-03FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application to add Claritin Chewable Grape and Bubblegum (loratadine) under the Claritin label, expanding the pr…
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FDA approval · 2018-12-21FDA Approved: CLARITIN — Supplemental Application (Bayer HealthCare LLC)
FDA approved a supplemental application for Claritin (loratadine) held by Bayer HealthCare LLC.
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FDA label_change · 2018-12-21FDA Approved: CLARITIN LIQUI-GELS — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Liqui-Gels (loratadine) by Bayer HealthCare LLC, indicating a labeling-related update.
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FDA approval · 2018-12-21FDA Approved: LORATADINE — Original Application (Bionpharma Inc.)
The FDA approved Bionpharma Inc.'s original ANDA for loratadine, authorizing a generic loratadine product to be marketed in the United State…
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FDA approval · 2018-11-20FDA Approved: ALLERGY RELIEF 24HR — Original Application (VELOCITY PHARMA LLC)
FDA approved the original application for Allergy Relief 24HR (levocetirizine dihydrochloride) from Velocity Pharma LLC. It is a generic ant…
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FDA label_change · 2018-10-11FDA Approved: CHILDRENS ZYRTEC — Supplemental Application (Kenvue Brands LLC)
FDA approved a supplemental labeling action for Children's Zyrtec (cetirizine hydrochloride) by Kenvue Brands LLC. The action updates the pr…
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FDA approval · 2018-08-22FDA Approved: DIPHENHYDRAMINE HYDROCHLORIDE — Original Application (Armas Pharmaceuticals Inc.)
FDA approved the original generic application for diphenhydramine hydrochloride from Armas Pharmaceuticals, making a generic diphenhydramine…
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FDA approval · 2018-08-13FDA Approved: FEXOFENADINE HYDROCHLORIDE — Original Application (Pioneer Life Sciences, LLC)
FDA approved a generic version of fexofenadine hydrochloride from Pioneer Life Sciences, LLC under an original ANDA, indicated for allergic …
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FDA approval · 2018-07-23FDA Approved: CLARITIN REDITABS — Supplemental Application (Bayer Healthcare LLC.)
FDA approved a supplemental application for Claritin RediTabs (loratadine) from Bayer, resulting in a labeling update for this product.
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FDA approval · 2018-07-20FDA Approved: CLARITIN LIQUI-GELS — Supplemental Application (Bayer HealthCare LLC.)
The FDA approved a supplemental application for Claritin Liqui-Gels (loratadine) from Bayer HealthCare LLC.
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FDA approval · 2018-06-29FDA Approved: LORATADINE — Original Application (Better Living Brands LLC)
FDA approves the original ANDA for loratadine oral by Better Living Brands LLC, authorizing its generic product.
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FDA approval · 2018-06-20FDA Approved: CLARITIN LIQUI-GELS — Supplemental Application (Bayer HealthCare LLC.)
The FDA approved a supplemental application to add CLARITIN LIQUI-GELS (loratadine) as a new dosage form for Claritin. This expands the prod…
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FDA label_change · 2018-06-04FDA Approved: CLARITIN LIQUI-GELS — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Liqui-Gels (loratadine) from Bayer HealthCare LLC.
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FDA approval · 2018-06-01FDA Approved: TOPCARE CHILDRENS ALLERGY — Supplemental Application (Topco Associates LLC)
The FDA approved a supplemental application for TOPCARE CHILDRENS ALLERGY (loratadine) from Topco Associates LLC, authorizing a labeling upd…
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FDA approval · 2018-05-30FDA Approved: CLARITIN — Supplemental Application (Bayer HealthCare LLC)
The FDA approved a supplemental application for Claritin (loratadine) filed by Bayer HealthCare LLC.