Common Cold
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Sign up freeTop drugs studied for this disease
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FDA approval · 2019-01-25FDA Approved: ADVIL ALLERGY AND CONGESTION RELIEF — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for ADVIL ALLERGY AND CONGESTION RELIEF, a combination product containing chlorpheniramine maleate, …
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FDA approval · 2018-12-04FDA Approved: BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, AND DEXTROMETHORPHAN HYDROBROMIDE — Original Application (Dr. Reddy's Labratories Inc.)
FDA approved an original ANDA for a generic cough-and-cold medication containing brompheniramine maleate, pseudoephedrine hydrochloride, and…
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FDA approval · 2018-11-30FDA Approved: DIPHENHYDRAMINE HYDROCHLORIDE — Supplemental Application (Armas Pharmaceuticals Inc.)
FDA approved a supplemental application for diphenhydramine hydrochloride from Armas Pharmaceuticals Inc.
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FDA approval · 2018-11-16FDA Approved: ALLERGY AND SINUS RELIEF — Original Application (Kroger Company)
FDA approved Kroger's original application for an OTC allergy and sinus relief product containing cetirizine hydrochloride and pseudoephedri…
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FDA approval · 2018-11-01FDA Approved: MUCUS RELIEF DM — Original Application (Dolgencorp, Inc. (DOLLAR GENERAL & REXALL))
FDA approved the original application for MUCUS RELIEF DM, a combination cough suppressant and expectorant (guaifenesin and dextromethorphan…
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FDA approval · 2018-07-31FDA Approved: CLARITIN-D 24 HOUR — Supplemental Application (Bayer HealthCare LLC.)
FDA approved a supplemental application for CLARITIN-D 24 HOUR (loratadine and pseudoephedrine sulfate) from Bayer HealthCare LLC.
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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 · 2018-04-19FDA 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 · 2018-03-05FDA Approved: MUCUS DM — Original Application (HyVee Inc)
FDA approved HyVee Inc's MUCUS DM as an original-application generic product containing dextromethorphan hydrobromide and guaifenesin for te…
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FDA approval · 2018-02-26FDA Approved: ADVIL ALLERGY AND CONGESTION RELIEF — Supplemental Application (Haleon US Holdings LLC)
FDA approves a supplemental application to market ADVIL ALLERGY AND CONGESTION RELIEF, a fixed-dose combination product containing chlorphen…
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FDA approval · 2017-12-29FDA Approved: GUAIFENESIN AND PSEUDOEPHEDRINE HCL — Original Application (Dr. Reddys Laboratories Limited)
FDA approved an original ANDA for guaifenesin and pseudoephedrine hydrochloride tablets from Dr. Reddys Laboratories Limited, establishing a…
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FDA approval · 2017-12-01FDA Approved: IBUPROFEN AND PSEUDOEPHEDRINE HCL — Original Application (Aurohealth LLC)
FDA approved Aurohealth LLC's ibuprofen and pseudoephedrine HCl combination as an Original Application. It is an over-the-counter product in…
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FDA approval · 2017-08-29FDA Approved: PROMETHAZINE AND PHENYLEPHRINE HCL, AND CODEINE PHOSPHATE — Supplemental Application (Amneal Pharmaceuticals LLC)
FDA approved a supplemental application for a generic combination product containing promethazine, phenylephrine, and codeine phosphate manu…
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FDA approval · 2017-07-13FDA Approved: MUCINEX DM MAXIMUM STRENGTH — Supplemental Application (RB Health (US) LLC)
FDA approved a supplemental application for Mucinex DM Maximum Strength (guaifenesin and dextromethorphan hydrobromide) by RB Health (US) LL…
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FDA approval · 2017-06-09FDA Approved: PSEUDOEPHEDRINE HCL — Original Application (Better Living Brands LLC)
FDA approved the original ANDA for pseudoephedrine HCl (Better Living Brands LLC), authorizing its marketing as an over-the-counter nasal de…
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FDA approval · 2017-04-28FDA Approved: ADVIL ALLERGY AND CONGESTION RELIEF — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for ADVIL ALLERGY AND CONGESTION RELIEF, a combination product containing chlorpheniramine maleate, …
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FDA approval · 2017-03-24FDA Approved: ADVIL SINUS CONGESTION AND PAIN — Supplemental Application (Haleon US Holdings LLC)
The FDA approved a supplemental application to market Advil Sinus Congestion and Pain, a combination ibuprofen and phenylephrine product fro…
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FDA approval · 2017-03-24FDA Approved: ADVIL ALLERGY AND CONGESTION RELIEF — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for Advil Allergy and Congestion Relief, a combination product containing chlorpheniramine maleate, …
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FDA approval · 2017-03-23FDA Approved: ADVIL COLD AND SINUS — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for Advil Cold and Sinus, a combination product of ibuprofen and pseudoephedrine hydrochloride. The …
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FDA approval · 2017-03-17FDA Approved: MUCUS RELIEF DM MAXIMUM STRENGTH — Original Application (Better Living Brands LLC)
The FDA approved the original ANDA for MUCUS RELIEF DM MAXIMUM STRENGTH, a combination product of guaifenesin and dextromethorphan hydrobrom…
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FDA approval · 2016-09-20FDA Approved: BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE — Original Application (Acella Pharmaceuticals, LLC)
FDA approved an original application for a generic combination product containing brompheniramine maleate, pseudoephedrine hydrochloride, an…
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FDA approval · 2016-08-25FDA Approved: TUXARIN — Supplemental Application (Mainpointe Pharmaceuticals)
FDA approved a supplemental application for TUXARIN (codeine phosphate and chlorpheniramine maleate) from Mainpointe Pharmaceuticals. The ap…
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FDA approval · 2016-03-15FDA Approved: ADVIL PM- DIPHENHYDRAMINE CITRATE AND IBUPROFEN TABLET, COATED — Supplemental Application (Lil Drug Store Products, Inc)
FDA approved a supplemental application for Advil PM tablets (ibuprofen and diphenhydramine citrate), expanding labeling to include this com…
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FDA approval · 2016-03-09FDA Approved: ZYRTEC-D — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for ZYRTEC-D, a combination of cetirizine hydrochloride and pseudoephedrine hydrochloride, submi…
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FDA approval · 2016-01-26FDA Approved: FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI — Supplemental Application (Dr.Reddy's Laboratories Limited)
FDA approved a supplemental application for Fexofenadine HCl and Pseudoephedrine HCl (Dr. Reddy's Laboratories Limited). This approval invol…