Focus: Accord Biopharma is a public specialty pharmaceutical company headquartered in Raleigh, NC, focused on biosimilars and specialty pharma across oncology, cardiovascular, neurology, immunology, and hematology. The company is heavily dependent on a single product generating 99% of revenue.
Profile data last refreshed 57m ago · AI intelligence enriched 3w ago
Accord Biopharma is a high-risk, low-growth specialty pharma play suitable only for risk-tolerant commercial or operations professionals seeking stability in a single-product cash cow, not for scientists or those seeking career advancement.
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.
Anchor product generating 99% of company revenue; post-LOE status indicates ongoing generic erosion and mature market position.
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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.
Generated by Claude from Accord Biopharma's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
Secondary revenue contributor with patent protection through 2033; minimal market share relative to Lenalidomide.
Mature cardiovascular product nearing loss of exclusivity; minimal revenue contribution.
Generic formulation post-LOE; commodity competitive landscape with minimal differentiation.
Duplicate generic formulation post-LOE; identical indication and revenue to ANDA #1.
Third generic amlodipine formulation; crowded market with eroding pricing and market share.
Fourth generic amlodipine SKU; smallest contributor among cardiovascular portfolio; indicates marginal product optimization.
Oncology product post-LOE with minimal market penetration; specialized indication limiting addressable market.
Chemotherapy agent in pre-launch phase; smallest revenue contributor with uncertain commercialization momentum.
78 discontinued, 63 duplicate formulations not shown
Based on last 4 crawl cycles
Source: USCIS H-1B Employer Data Hub
Manufacturing discontinuations of key products (Methotrexate) and active drug shortages suggest supply chain vulnerability and regulatory compliance challenges that could trigger operational disruptions and workforce reductions.
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