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Last Updated: December 19, 2025

Suppliers and packagers for saxenda


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saxenda

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Novo SAXENDA liraglutide SOLUTION;SUBCUTANEOUS 206321 NDA Novo Nordisk 0169-2800-15 5 SYRINGE, PLASTIC in 1 CARTON (0169-2800-15) / 3 mL in 1 SYRINGE, PLASTIC 2014-12-31
Novo SAXENDA liraglutide SOLUTION;SUBCUTANEOUS 206321 NDA Novo Nordisk 0169-2800-90 1 SYRINGE, PLASTIC in 1 CARTON (0169-2800-90) / 3 mL in 1 SYRINGE, PLASTIC 2014-12-31
Novo SAXENDA liraglutide SOLUTION;SUBCUTANEOUS 206321 NDA Novo Nordisk 0169-2800-97 1 SYRINGE, PLASTIC in 1 CARTON (0169-2800-97) / 3 mL in 1 SYRINGE, PLASTIC 2014-12-31
Novo SAXENDA liraglutide SOLUTION;SUBCUTANEOUS 206321 NDA A-S Medication Solutions 50090-4257-0 5 SYRINGE, PLASTIC in 1 CARTON (50090-4257-0) / 3 mL in 1 SYRINGE, PLASTIC 2014-12-31
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers for the Pharmaceutical Drug: Saxenda

Last updated: July 27, 2025

Introduction

Saxenda, marketed by Novo Nordisk, is a prescription medication widely utilized for weight management and obesity treatment. Its active ingredient, liraglutide, is a glucagon-like peptide-1 (GLP-1) receptor agonist. As the landscape of obesity management expands, understanding the suppliers involved in Saxenda’s production, distribution, and associated components offers critical insights for stakeholders ranging from healthcare providers to investors. This article provides a comprehensive overview of Saxenda’s supply chain, highlighting primary suppliers, manufacturing processes, and strategic considerations.

Manufacturing and Raw Material Suppliers

Active Pharmaceutical Ingredient (API) Supply

Liraglutide, the active compound in Saxenda, is a complex peptide synthesized via recombinant DNA technology in biopharmaceutical manufacturing facilities. The primary suppliers for the raw materials and the API include contract manufacturing organizations (CMOs) with specialized facilities capable of peptide synthesis at scale.

  • Fujifilm Kyowa Kirin Biologics: Notably involved in the manufacturing of pharmaceuticals involving peptide synthesis, this Japanese company supplies active ingredients and intermediates for GLP-1 analogs, including liraglutide, although direct confirmation for Saxenda-specific API sourcing remains proprietary.

  • Samsung Biologics: A South Korean CMO with advanced facilities for biologics, Samsung offers peptide manufacturing services for pharmaceutical clients, potentially including liraglutide production, given their expanding footprint into complex biologic APIs.

  • Lonza: A leading Swiss CMOs in biopharmaceuticals, Lonza provides peptide synthesis and biologic manufacturing, making it a probable supplier of liraglutide API components for Saxenda.

Excipients and Formulation Components

  • Segmented Suppliers: Excipients such as monobasic and dibasic sodium phosphate, phenol, and water for injection are sourced from diverse chemical suppliers, including global players like Thermo Fisher Scientific and Merck KGaA.

Supply Chain and Distribution Network

Global Distribution Partners

Novo Nordisk leverages a complex distribution network to ensure Saxenda’s availability worldwide. The company collaborates with global logistics firms specialized in pharmaceutical distribution, such as DHL and FedEx, to handle temperature-sensitive shipments.

  • Distribution Hubs: Major warehouses are strategically located in North America, Europe, and Asia-Pacific to facilitate timely delivery and inventory management, with suppliers like DHL providing refrigerated logistics solutions.

Regional Suppliers and Distributors

Regional distribution agreements often involve third-party logistics (3PL) providers and local distributors, which vary by market. For instance, in the U.S., Novo Nordisk collaborates with specialty pharmacies and healthcare providers, while in emerging markets, local distributors maintain supply chains.

Regulatory and Certification Considerations

Suppliers involved in API manufacturing and excipients must comply with rigorous regulatory standards, including:

  • Good Manufacturing Practices (GMP): Required for all API and excipient suppliers.
  • FDA and EMA approvals: Ensure that manufacturing sites are authorized to produce pharmaceutical-grade components.
  • QS (Quality Systems) Certification: Validates that suppliers maintain high manufacturing standards.

Strategic Supplier Relationships and Risks

The complexity of Saxenda’s production underscores the importance of dependable suppliers. Novo Nordisk’s strategic risk mitigation includes diversifying sources for APIs and excipients, maintaining multiple approved suppliers for key components, and closely monitoring geopolitical risks affecting supply continuity.

Emerging Trends and Impacts on Supply

  • Supply Chain Resilience: The COVID-19 pandemic emphasized the need for resilient supply chains, prompting companies to diversify manufacturing sites and increase inventory buffers.

  • Biologics Specialization: As peptide-based therapeutics become more prevalent, suppliers investing in biotech manufacturing capabilities will see increased demand.

  • Sustainability: Suppliers that adopt environmentally friendly manufacturing practices could gain market advantage, aligning with corporate social responsibility initiatives.

Competitive Landscape of Suppliers

While Novo Nordisk maintains direct control over critical supply components, reliance on top-tier CMOs and chemical suppliers remains essential. Competitive pressures, patent protections, and geopolitical factors influence supplier selection and stability.

Conclusion

The supply chain for Saxenda spans multiple tiers, from raw material sourcing and peptide synthesis to formulation, packaging, and distribution. The primary API suppliers are leading global CMOs capable of peptide manufacturing, with excipients procured from established chemical suppliers. The strategic importance of supplier diversity and regulatory compliance underscores the robustness needed to maintain Saxenda’s supply integrity in the competitive pharmaceutical market.


Key Takeaways

  • Saxenda’s production relies heavily on specialized biopharmaceutical CMOs with peptide synthesis expertise.
  • Geographic diversification of suppliers mitigates risks associated with geopolitical instability and supply disruptions.
  • Regulatory compliance (GMP, FDA, EMA approval) is critical in supplier selection.
  • Supply chain resilience has gained importance, with companies adopting diversification and inventory strategies.
  • Emerging trends favor suppliers investing in sustainable and advanced biologic manufacturing capabilities.

Frequently Asked Questions (FAQs)

  1. Who are the main contract manufacturers for Saxenda’s API?
    While specific contracts are proprietary, leading biologics CMOs like Samsung Biologics, Lonza, and Fujifilm Kyowa Kirin are potential suppliers due to their specializations in peptide synthesis.

  2. Are there multiple suppliers for Saxenda’s excipients?
    Yes, excipients such as sodium phosphate and phenol are sourced from multiple chemical suppliers like Thermo Fisher Scientific and Merck KGaA to ensure supply security.

  3. How does Novo Nordisk manage supply chain risks for Saxenda?
    The company employs diversified sourcing, regional distribution hubs, and stringent regulatory oversight to ensure supply continuity and mitigate disruptions.

  4. What role do regulatory agencies play in Saxenda’s supply chain?
    Agencies like the FDA and EMA certify manufacturing sites and enforce GMP standards, ensuring supply chain partners maintain high-quality manufacturing practices.

  5. How might emerging biotech trends impact Saxenda’s supply chain?
    Increased demand for peptide-based therapeutics will likely drive investment in advanced biologics manufacturing, expanding the pool of capable suppliers and enhancing supply chain resilience.


References

  1. Novo Nordisk’s official product information on Saxenda.
  2. Industry reports on biopharmaceutical manufacturing and supply chain strategies.
  3. Public disclosures from contract manufacturing organizations (CMOs) regarding peptide synthesis capabilities.
  4. Regulatory agency guidelines on pharmaceutical manufacturing standards.
  5. Market analyses on the global supply chain trends in biologics and peptide therapeutics.

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