Focus: Bausch + Lomb is a public specialty pharma company headquartered in New Jersey with a dominant focus on ophthalmology therapeutics and devices. The company derives 50% of revenue from its flagship dry eye drug XIIDRA, positioning it as a specialized player in the eye care market.
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Generated by Claude from Bausch + Lomb's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
Automated analysis based on publicly available data (FDA, SEC, ClinicalTrials.gov). May be incomplete or delayed. This score does not reflect insider knowledge and should not be used as the sole basis for investment or employment decisions.
Flagship product representing 50% of company revenue; lymphocyte function-associated antigen antagonist with stable peak-stage commercial performance and extended patent protection through 2033.
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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.
Second-largest revenue contributor facing significant patent cliff risk in February 2029; near-term generic erosion expected to accelerate competitive pressure and revenue decline.
NSAID anti-inflammatory ophthalmic suspension in peak commercial phase with patent protection extending to November 2033; stable revenue contributor in surgical inflammation management.
Azole antifungal topical with peak-stage revenue and extended exclusivity through April 2035; represents diversification into dermatological indication within ophthalmology portfolio.
Non-ophthalmology psychiatric agent approaching loss of exclusivity; represents legacy portfolio component facing generic competition with minimal patent cliff visibility in the data.
Generic prostaglandin analog in post-LOE phase; mature competitive glaucoma market with limited differentiation and continued revenue erosion expected.
Corticosteroid ophthalmic suspension in peak phase with long patent tail to December 2036; moderate revenue contributor with solid IP protection in inflammation/allergy management.
Post-LOE psychiatric formulation with patent cliff already passed (June 2026); minimal strategic value in ophthalmology-focused organization with ongoing revenue decline.
Lower-dose ophthalmic corticosteroid suspension in allergy indication facing LOE; smaller revenue contributor with increasing generic competition in crowded allergic conjunctivitis market.
181 discontinued, 67 duplicate formulations not shown
+26 more products with revenue data
Bausch Lomb (TSX:BLCO): Eye Health Growth In Healthcare - Kalkine Media
Bausch Lomb (TSX:BLCO): Eye Health Growth In Healthcare Kalkine Media
Bausch + Lomb Launches Miebo for Dry Eye Disease - Managed Healthcare Executive
Bausch + Lomb Launches Miebo for Dry Eye Disease Managed Healthcare Executive
Robinson Pharma, Inc. Receives "Above and Beyond" Supplier Award from Bausch + Lomb for September 2026 - KITV
Robinson Pharma, Inc. Receives "Above and Beyond" Supplier Award from Bausch + Lomb for September 2026 KITV
FDA drops warning letter on Bausch & Lomb, citing contamination concerns - Fierce Pharma
FDA drops warning letter on Bausch & Lomb, citing contamination concerns Fierce Pharma
FDA warning letter accuses Bausch & Lomb of lacking commitment to remediation - BioSpace
FDA warning letter accuses Bausch & Lomb of lacking commitment to remediation BioSpace
Bausch + Lomb progresses dry eye candidate to Phase III despite mixed data - Clinical Trials Arena
Bausch + Lomb progresses dry eye candidate to Phase III despite mixed data Clinical Trials Arena
Showing 6 of 10 news items
No open positions listed yet. Check their careers page directly.
Based on last 4 crawl cycles
Source: USCIS H-1B Employer Data Hub
Source: state DOL filings, aggregated via Big Local News
Recent peer-reviewed publications with author affiliations at this company
+63 more products
Two WARN Act filings within 13 months (400 + 49 employees) combined with FDA warning letters (September 2026) citing contamination and inadequate remediation indicate active organizational stress, operational challenges, and possible continued workforce reductions.
Showing 5 of 10 publications
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