NDAORALTABLET, EXTENDED RELEASE
Approved
Nov 1994
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Clinical Trials
3
Data completeness
4/8 — Partial
CLARITIN-D (loratadine and pseudoephedrine sulfate) by Bayer. Approved for these symptoms due to hay fever, other upper respiratory allergies: sneezing itchy, watery eyes runny nose itching of the nose and 4 more indications. First approved in 1994.
Drug data last refreshed 19h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
Claritin-D is an oral extended-release tablet combining loratadine (a non-sedating antihistamine) and pseudoephedrine sulfate (a nasal decongestant). It treats allergic rhinitis symptoms including sneezing, itchy/watery eyes, runny nose, and nasal congestion from hay fever and upper respiratory allergies. The dual mechanism addresses both histamine-mediated allergic responses and nasal swelling to restore freer breathing.
LOE Approaching
Product is in late lifecycle maturity with significant competitive pressure (30/100 intensity), indicating team focus likely on defending market share and operational efficiency rather than expansion.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.