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 5h ago · AI intelligence enriched 6d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
CLARITIN-D is a combination oral tablet containing loratadine (a non-sedating antihistamine) and pseudoephedrine sulfate (a nasal decongestant) in extended-release formulation. It treats symptoms of hay fever and upper respiratory allergies including sneezing, itching, watery eyes, runny nose, nasal congestion, and sinus pressure. The drug works by blocking histamine receptors to reduce allergic symptoms while the decongestant reduces swelling of nasal passages to restore freer breathing.
LOE Approaching
Product is entering loss-of-exclusivity phase with elevated competitive pressure (30/100), signaling potential contraction of brand team resources and shift toward defensive marketing strategies.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Worked on CLARITIN-D at Bayer? Share your interview experience or compensation data (+7 days Pro)
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.