Allergic Rhinitis
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Sign up freeTop drugs studied for this disease
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FDA approval · 2018-07-20FDA Approved: CLARITIN CHEWABLE GRAPE AND BUBBLEGUM — Supplemental Application (Bayer HealthCare LLC.)
The FDA approved a supplemental application for Claritin Chewable Grape and Bubblegum (loratadine) from Bayer HealthCare LLC.
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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 · 2018-07-20FDA Approved: CETIRIZINE HYDROCHLORIDE (ALLERGY) — Original Application (RITE AID CORPORATION)
FDA approves Rite Aid's original ANDA for cetirizine hydrochloride (allergy). It is a generic antihistamine used to treat allergic rhinitis.
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FDA approval · 2018-07-05FDA Approved: CLARITIN — Supplemental Application (Bayer HealthCare LLC)
The FDA approved a supplemental application for Claritin (loratadine) filed by Bayer HealthCare LLC.
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FDA approval · 2018-07-03FDA Approved: BUDESONIDE — Original Application (Actavis Pharma, Inc.)
FDA approved the original application for Budesonide from Actavis Pharma, Inc. (ANDA205457).
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FDA approval · 2018-07-02FDA Approved: MONTELUKAST SODIUM — Original Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved the original ANDA for montelukast sodium from Unichem Pharmaceuticals (USA), Inc., establishing a generic version of this asthm…
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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 approval · 2018-06-08FDA Approved: PROMETHAZINE AND PHENYLEPHRINE HCL, AND CODEINE PHOSPHATE — Supplemental Application (Amneal Pharmaceuticals LLC)
FDA approved a supplemental application for PROMETHAZINE AND PHENYLEPHRINE HCL, AND CODEINE PHOSPHATE by Amneal Pharmaceuticals 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.
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FDA approval · 2018-05-25FDA Approved: NASAL ALLERGY — Supplemental Application (Kroger Company)
The FDA approved a supplemental application for a generic nasal spray product called NASAL ALLERGY containing triamcinolone acetonide, manuf…
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FDA approval · 2018-05-21FDA Approved: LEVOCETIRIZINE DIHYDROCHLORIDE — Supplemental Application (Dr. Reddy's Laboratories Inc.)
The FDA approved a supplemental application for a generic version of levocetirizine dihydrochloride from Dr. Reddy's Laboratories Inc.
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FDA approval · 2018-05-18FDA Approved: MONTELUKAST SODIUM — Supplemental Application (Accord Healthcare Inc.)
FDA approved Accord Healthcare Inc.'s supplemental application for Montelukast Sodium.
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FDA approval · 2018-05-18FDA Approved: MONTELUKAST — Supplemental Application (BluePoint Laboratories)
The FDA approved a supplemental application for montelukast submitted by BluePoint Laboratories under ANDA 203366. The decision denotes appr…
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FDA approval · 2018-05-14FDA Approved: CLARITIN ALLERGY — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for Claritin Allergy (loratadine) from Bayer HealthCare LLC, approving the supplemental action relat…
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FDA approval · 2018-05-14FDA Approved: MONTELUKAST SODIUM — Supplemental Application (Unichem Pharmaceuticals (USA), Inc.)
FDA approved a supplemental application for montelukast sodium from Unichem Pharmaceuticals (USA), Inc., indicating approval of an additiona…
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FDA approval · 2018-04-19FDA Approved: CLARINEX-D 12 HOUR — Supplemental Application (Organon LLC)
FDA has approved a supplemental application for CLARINEX-D 12 HOUR (desloratadine and pseudoephedrine sulfate) submitted by Organon LLC.
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FDA approval · 2018-04-16FDA Approved: LORATADINE — Original Application (Chain Drug Consortium, LLC)
The FDA approved the original application for loratadine filed by Chain Drug Consortium, LLC, enabling a generic loratadine product to be ma…
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FDA approval · 2018-04-16FDA Approved: LORATADINE — Original Application (Wal-Mart Stores, Inc)
FDA approves Wal-Mart Stores, Inc.'s original ANDA for loratadine (generic antihistamine) to treat allergy symptoms.
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FDA approval · 2018-04-11FDA Approved: LORATADINE ODT — Original Application (Aurohealth LLC)
FDA approved a generic loratadine orally disintegrating tablet (LORATADINE ODT) under ANDA 208477 with Aurohealth LLC as the sponsor. The pr…
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FDA approval · 2018-04-02FDA Approved: XYZAL — Supplemental Application (Chattem, Inc.)
FDA approved a supplemental application for XYZAL (levocetirizine dihydrochloride) filed by Chattem, Inc. The action confirms changes to the…
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FDA approval · 2018-03-30FDA Approved: QNASL — Supplemental Application (Teva Respiratory, LLC)
The FDA approved a supplemental application for QNASL (beclomethasone dipropionate) submitted by Teva Respiratory, LLC.
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FDA approval · 2018-03-26FDA Approved: ASMANEX HFA — Supplemental Application (Organon LLC)
FDA approved a supplemental NDA for ASMANEX HFA (mometasone furoate) from Organon LLC, authorizing changes via a supplemental application.
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FDA approval · 2018-03-19FDA Approved: XHANCE — Supplemental Application (OptiNose US, Inc.)
FDA approved a supplemental application for XHANCE (fluticasone propionate) submitted by OptiNose US, Inc. The approval is categorized as a …