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 17h ago · AI intelligence enriched 3w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
CLARITIN-D is an oral extended-release combination tablet containing loratadine (a non-sedating antihistamine) and pseudoephedrine sulfate (a nasal decongestant). It treats symptoms of hay fever and upper respiratory allergies including sneezing, itchy/watery eyes, runny nose, nasal congestion, and sinus pressure. The drug works by blocking histamine receptors to reduce allergic symptoms while constricting nasal blood vessels to relieve congestion.
LOE Approaching
As a mature brand approaching loss of exclusivity with moderate competitive pressure (30%), commercial teams should focus on brand loyalty and line extension strategies rather than market 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.