Focus: Accord Biopharma is a publicly traded specialty pharmaceutical company based in Raleigh, NC, focused on biosimilars and generic/branded drugs across oncology, cardiovascular, and immunology indications.
Profile data last refreshed 12h ago · AI intelligence enriched 3w ago
Stable — net +3 jobs in 30d
4 added, 1 removed. Backfill posture.
High-risk, revenue-dependent opportunity suitable only for commercial or operations professionals seeking stability; unsuitable for those prioritizing scientific innovation, career growth, or R&D involvement.
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.
Core revenue driver (99% of company revenue) but facing post-LOE erosion; immunomodulatory mechanism targets hematopoietic tumors and MDS via cereblon pathway.
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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.
NDA product with patent protection until 2033; minor revenue contributor but represents diversification away from lenalidomide dependency.
Original NDA formulation facing LOE with multiple ANDA competitors already in market; calcium channel blocker with established efficacy but limited differentiation.
ANDA generic formulation in post-LOE phase; part of three ANDA entries totaling $761K in Part D spending across hypertension indications.
Duplicate ANDA entry for amlodipine generic; reflects fragmented portfolio of low-value post-LOE generics with minimal differentiation.
Third amlodipine ANDA formulation; demonstrates company reliance on commodity generic blood pressure agents with eroding margins.
Fourth amlodipine ANDA variant generating lowest Part D revenue; indicative of portfolio bloat in mature generic space.
mTOR inhibitor ANDA for oncology; minimal revenue contribution but represents rare specialty oncology generic position.
Chemotherapy ANDA in pre-launch stage; platinum-based antineoplastic with potential upside if successfully commercialized, but minimal current revenue.
78 discontinued, 63 duplicate formulations not shown
Based on last 4 crawl cycles
Source: USCIS H-1B Employer Data Hub
Company is not on FDA warning list but participates in drug shortage ecosystem (methotrexate manufacturing discontinuation); stable regulatory compliance but limited visibility on workforce stability.
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