Suppliers and packagers for tarceva

tarceva

Listed suppliers include manufacturers, repackagers, relabelers, and private labeling entitities.

Applicant	Tradename	Generic Name	Dosage	NDA	NDA/ANDA	Supplier	Package Code	Package	Marketing Start
Osi Pharms	TARCEVA	erlotinib hydrochloride	TABLET;ORAL	021743	NDA	Genentech, Inc.	50242-062-01	30 TABLET in 1 BOTTLE (50242-062-01)	2005-04-30
Osi Pharms	TARCEVA	erlotinib hydrochloride	TABLET;ORAL	021743	NDA	Genentech, Inc.	50242-063-01	30 TABLET in 1 BOTTLE (50242-063-01)	2005-04-30
Osi Pharms	TARCEVA	erlotinib hydrochloride	TABLET;ORAL	021743	NDA	Genentech, Inc.	50242-064-01	30 TABLET in 1 BOTTLE (50242-064-01)	2005-04-30

Suppliers for the Pharmaceutical Drug: TARCEVA (Erlotinib)

Last updated: July 30, 2025

Introduction

TARCEVA (erlotinib) is an oral targeted cancer therapy primarily indicated for non-small cell lung cancer (NSCLC) and pancreatic cancer. Since its approval by the FDA in 2004, TARCEVA has become a mainstay in oncology treatment protocols. As a pioneering epidermal growth factor receptor (EGFR) inhibitor, its supply chain integrity is vital for maintaining global drug availability amidst rising demand. This article provides a comprehensive overview of TARCEVA suppliers, analyzing manufacturing sources, distribution channels, and supply chain dynamics crucial for industry stakeholders.

Manufacturers and Patent Holders

Eli Lilly and Company holds the original patent and manufacturing rights for TARCEVA (erlotinib). The primary manufacturing facilities are located in the United States and Europe, aligned with regulatory standards for pharmaceutical production.

Eli Lilly & Company, headquartered in Indianapolis, Indiana, is the sole patent holder and primary producer. The company's manufacturing capabilities include advanced facilities equipped for sterile and non-sterile drug production, adhering to Good Manufacturing Practices (GMP) prescribed by regulators such as the FDA and EMA.

Global Supply and Licensing Agreements

While Eli Lilly retains exclusive rights, strategic licensing arrangements and partnerships have expanded TARCEVA’s global distribution:

• In Asia and emerging markets, Eli Lilly often sublicenses manufacturing or collaborates with regional pharmaceutical companies to enhance access and reduce costs.
• In China, for example, partnership with local firms like Jiangsu Hengrui Medicine has facilitated broad market penetration, although Hengrui does not produce TARCEVA but may develop similar molecules.

Ongoing licensing agreements enable Eli Lilly to extend its supply chain reach, particularly in countries with complex regulatory environments, ensuring consistent drug availability.

Contract Manufacturing and Outsourcing

Although Eli Lilly controls primary manufacturing of TARCEVA, it relies on a network of Contract Manufacturing Organizations (CMOs) to meet global demand:

• CMOs such as Fujifilm Diosynth Biotechnologies and Thermo Fisher Scientific have been involved in the production of active pharmaceutical ingredients (API) or formulation stages.
• Contract manufacturing allows Eli Lilly to scale production efficiently, mitigate risks such as supply disruptions, and adhere to regional regulatory requirements (e.g., EMA, FDA).

Supply Chain Challenges and Risks

The supply chain for TARCEVA faces specific challenges:

• API Shortages: As TARCEVA's active pharmaceutical ingredient is complex to synthesize, fluctuations in API supply can impact production. This issue has been evident during global disruptions such as COVID-19, which strained supply chains worldwide.
• Regulatory Delays: Changes in manufacturing standards or geopolitical tensions can delay approval of manufacturing sites, constraining supply.
• Patent Expirations and Generics: Although Eli Lilly possesses the original patent, generic manufacturers have begun producing erlotinib post-expiration in certain markets, complicating the supply landscape and emphasizing the importance of patent protection and patent litigation.

Generic and Biosimilar Competition

After patent expiration in key markets, several pharmaceutical manufacturers have started to produce generic erlotinib, increasing market competition:

• Teva Pharmaceutical Industries and Mylan entered the market shortly after patent expiry, providing lower-cost options.
• The proliferation of generics has impacted Eli Lilly’s market share and its supply planning, with some generic suppliers sourcing APIs from different regions, emphasizing the importance of diversified sourcing strategies.

Distribution Channels

TARCEVA’s distribution is managed through licensed wholesalers, specialty pharmacies, and direct distribution channels, depending on regional healthcare infrastructures:

• In North America and Europe, Eli Lilly collaborates with major distributors such as McKesson, Cardinal Health, and Alliance Healthcare.
• In emerging markets, local distributors and government procurement programs play a crucial role, often involving tender-based procurement processes to ensure drug affordability and availability.

The drugs are shipped in temperature-controlled logistics to preserve stability, especially in regions with challenging climatic conditions.

Market Dynamics and Future Outlook

The future supply landscape of TARCEVA will be influenced by:

• Patent Litigation and Exclusivity Periods: Patent protections extend until 2028 in many jurisdictions, delaying generic entry.
• Synthesis Innovations: Advances in API manufacturing techniques could alter supply chain configurations, potentially reducing costs and increasing resilience.
• Emerging Market Growth: Increasing cancer prevalence in Asia-Pacific and Latin America boosts demand, prompting Eli Lilly and regional partners to expand manufacturing and distribution capabilities accordingly.
• Regulatory Environment: Stringent manufacturing standards and approval processes demand continuous compliance, which can impact supply chain stability.

Conclusion

Eli Lilly remains the primary supplier of TARCEVA, leveraging a network of manufacturing facilities and strategic licensing to maintain global distribution. The emergence of generics post-patent expiry introduces new competitors, diversifying the supply landscape but also posing risks related to API sourcing and regulatory compliance. Ensuring a resilient supply chain involves managing regional distribution partnerships, expanding manufacturing capacity, and navigating patent protections.

Key Takeaways

• Eli Lilly maintains exclusive control over TARCEVA’s manufacturing with a network of CMOs to meet global demand.
• Contract manufacturing and regional licensing agreements are crucial to expanding access and mitigating supply risks.
• Patent expiration has heightened generic competition, impacting market dynamics and supply security.
• Regional distribution strategies are tailored to local healthcare infrastructures, affecting availability.
• Future supply resilience hinges on innovations in drug synthesis, patent extensions, and strategic regional expansion.

FAQs

1. Who are the primary suppliers of TARCEVA globally?
Eli Lilly and Company is the sole patent holder and primary supplier, utilizing a network of Contract Manufacturing Organizations (CMOs) to produce active pharmaceutical ingredients and formulations across various regions.

2. Are there generic versions of TARCEVA available?
Yes. Following patent expiration in several markets, generic manufacturers like Teva and Mylan have begun producing erlotinib, increasing market competition and supply options.

3. What are the main risks to TARCEVA’s supply chain?
Risks include API shortages, manufacturing delays due to regulatory issues, geopolitical tensions, and patent litigation. Supply disruptions are more pronounced in emerging markets with complex logistics.

4. How does Eli Lilly ensure TARCEVA’s supply in emerging markets?
Through regional licensing agreements, local manufacturing partnerships, and collaboration with distributors, Eli Lilly adapts to local regulatory and infrastructure challenges to maintain availability.

5. What are the future prospects for TARCEVA’s supply chain?
Advancements in synthesis technologies, patent extensions, and strategic global expansion will be key. Emphasizing diversified sourcing and regional manufacturing will further enhance supply resilience.

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Sources

1. Eli Lilly & Company. "TARCEVA (Erlotinib) Prescribing Information," 2022.
2. U.S. Food and Drug Administration (FDA). "TARCEVA Approval History," 2004.
3. Global Data. "Pharmaceutical Market Dynamics," 2022.
4. Patent and Trademark Office Data. "Erlotinib Patent Status," 2022.
5. MarketWatch. "Generic Competition and Market Share," 2022.