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Last Updated: December 12, 2025

Suppliers and packagers for generic pharmaceutical drug: leuprolide acetate


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leuprolide acetate

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

Applicant Tradename Generic Name Dosage NDA NDA/ANDA Supplier Package Code Package Marketing Start
Invagen Pharms LEUPROLIDE ACETATE FOR DEPOT SUSPENSION leuprolide acetate FOR SUSPENSION;INTRAMUSCULAR 205054 NDA CIPLA USA INC. 69097-909-50 1 KIT in 1 CARTON (69097-909-50) * 2 mL in 1 VIAL, SINGLE-DOSE (69097-950-32) * 2 mL in 1 SYRINGE (69097-960-31) 2022-07-15
Invagen Pharms LEUPROLIDE ACETATE FOR DEPOT SUSPENSION leuprolide acetate FOR SUSPENSION;INTRAMUSCULAR 205054 NDA Avyxa Pharma, LLC 83831-134-01 1 KIT in 1 CARTON (83831-134-01) * 2 mL in 1 VIAL, SINGLE-DOSE (83831-150-22) * 2 mL in 1 SYRINGE (83831-135-02) 2025-03-26
Abbvie Endocrine Inc LUPRON DEPOT leuprolide acetate INJECTABLE;INJECTION 020011 NDA AbbVie Inc. 0074-3641-03 1 KIT in 1 CARTON (0074-3641-03) * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET 1990-10-22
Abbvie Endocrine Inc LUPRON DEPOT leuprolide acetate INJECTABLE;INJECTION 020011 NDA AbbVie Inc. 0074-3641-71 1 KIT in 1 CARTON (0074-3641-71) * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET 1990-10-22
Abbvie Endocrine Inc LUPRON DEPOT leuprolide acetate INJECTABLE;INJECTION 019732 NDA AbbVie Inc. 0074-3642-03 1 KIT in 1 CARTON (0074-3642-03) * 1 mL in 1 SYRINGE * 1 SWAB in 1 PACKET 1989-01-26
>Applicant >Tradename >Generic Name >Dosage >NDA >NDA/ANDA >Supplier >Package Code >Package >Marketing Start

Suppliers for the Pharmaceutical Drug: Leuprolide Acetate

Last updated: July 29, 2025

Introduction

Leuprolide acetate is a synthetic analog of gonadotropin-releasing hormone (GnRH) widely used in the management of hormone-dependent conditions, including prostate cancer, endometriosis, central precocious puberty, and uterine fibroids. The global demand for this drug necessitates a robust supply chain comprising multiple manufacturers, both branded and generic. Understanding the landscape of suppliers for leuprolide acetate provides insight into market competition, pricing dynamics, supply security, and regulatory considerations. This article offers a comprehensive analysis of key suppliers, highlighting their manufacturing capabilities, market positioning, and strategic importance.

Global Market Overview

Leuprolide acetate is produced through complex peptide synthesis processes, demanding high-quality manufacturing standards aligned with regulatory authorities such as the FDA, EMA, and PMDA. The drug's essential role in hormone therapy sustains significant demand, fostered by the aging population, expanding indications, and ongoing research. Major suppliers span regions including North America, Europe, and Asia, reflecting a geographically diversified supply chain.

Major Suppliers of Leuprolide Acetate

1. AbbVie Inc.

Overview:
AbbVie remains a prominent player in the leuprolide acetate market, offering the brand-name drug, Lupron Depot. With a robust R&D infrastructure and GMP-compliant manufacturing facilities, AbbVie ensures high-quality supplies globally.

Manufacturing Capabilities:
AbbVie’s manufacturing centers in the United States and Europe are equipped to produce various formulations of leuprolide acetate, including depot injections and nasal sprays. These facilities adhere to strict regulatory standards, supporting continuous supply and product innovation.

Market Presence:
AbbVie’s longstanding market position provides a stable supply source, with strong distribution networks. Their extensive pharmacovigilance ensures ongoing safety and efficacy monitoring.

2. Pfizer Inc.

Overview:
Pfizer manufactures leuprolide acetate under the brand Lupron outside the US, primarily serving markets in Europe and emerging economies. It maintains a well-established peptide synthesis division capable of large-scale production.

Manufacturing Capabilities:
Pfizer’s facilities in Europe utilize advanced peptide synthesis and sterilization procedures, meeting European Medicines Agency (EMA) standards. They have also invested in biosimilar development to expand access.

Market Role:
While Pfizer does not generally operate as a primary supplier in North America, their global footprint makes them a key competitor and supply contributor in international markets.

3. Takeda Pharmaceutical Company

Overview:
Takeda manufactures leuprolide acetate as part of its hormone therapy portfolio, especially targeting Asian and Latin American markets. Their global manufacturing network emphasizes quality and cost efficiency.

Manufacturing Capabilities:
Takeda’s facilities in Japan, India, and other regions enable large-volume peptide production, incorporating modern purification and formulation techniques to ensure product stability and bioavailability.

Market Role:
Takeda’s competitive pricing and localized manufacturing support access in emerging markets, offering affordable alternatives to branded formulations.

4. Sun Pharmaceutical Industries Ltd.

Overview:
Sun Pharma, an Indian-based pharmaceutical giant, supplies generic versions of leuprolide acetate, addressing the growing demand for cost-effective alternatives worldwide.

Manufacturing Capabilities:
Sun Pharma’s advanced peptide synthesis plants in India follow cGMP standards and utilize innovative purification methods to meet international quality requirements.

Market Role:
As a leading supplier of generic injectables, Sun Pharma plays a crucial role in increasing the drug’s affordability and availability, especially in developing regions.

5. Others: Teva Pharmaceuticals and Sandoz

Teva Pharmaceuticals:
Specializes in generic injectables, including leuprolide acetate, offering reliable supply in North America and Europe. Their manufacturing units employ high-throughput peptide synthesis technology.

Sandoz (Novartis):
Provides biosimilar leuprolide acetate formulations, expanding access via competitive pricing and diversified supply channels.

Emerging and Regional Suppliers

Besides the major players, several regional manufacturers and contract manufacturing organizations (CMOs) contribute to the supply ecosystem, especially for mid-sized markets or private-label products. These include organizations in China, South Korea, and Eastern Europe, often licensed or partnered through technology transfer agreements to ensure quality compliance.

Regulatory and Quality Considerations

Manufacturers aiming to supply leuprolide acetate face rigorous regulatory scrutiny concerning peptide purity, endotoxin levels, sterility, and bioequivalence. Ensuring Good Manufacturing Practice (GMP) compliance is fundamental for market approval and sustained supply.

Additionally, patent exclusivity and licensing agreements influence the competitive landscape. As patents for the original formulations lapse, generic manufacturers can further penetrate markets, leading to increased competition and lower prices.

Supply Chain and Market Dynamics

The supply of leuprolide acetate is sensitive to manufacturing disruptions, raw material availability (notably peptide synthesis reagents), and regulatory changes. Supply security hinges on diversified manufacturing sites and strategic stockpiling. The entry of biosimilars and generics continues to reshape the competitive landscape, emphasizing affordability and regional accessibility.

Key Challenges

  • Manufacturing Complexity: The peptide synthesis process is intricate and requires precision to ensure bioactivity and safety.

  • Regulatory Hurdles: Cross-border approval processes and quality standards can delay market entry.

  • Supply Chain Disruptions: Raw material shortages, geopolitical issues, and pandemic impacts threaten supply continuity.

Future Outlook

The leuprolide acetate market is poised for growth driven by expanding indications and evolving treatment protocols. Investments in biosimilar development and advanced manufacturing techniques will likely enhance supply resilience, while regulatory harmonization could streamline approvals. However, market players must navigate patent landscapes and quality standards to maintain competitiveness.

Key Takeaways

  • Leading suppliers of leuprolide acetate include AbbVie (Lupron Depot), Pfizer, Takeda, Sun Pharma, and regional generic manufacturers.
  • Manufacturing requires high technical expertise, rigorous quality control, and compliance with global standards.
  • Competition is intensifying with the advent of biosimilars and generics, enhancing affordability.
  • Supply stability depends on diversified manufacturing sites and raw material access.
  • Regulatory environments significantly influence market entry, pricing, and supply continuity.

FAQs

Q1: What are the primary global suppliers of leuprolide acetate?
A1: Major suppliers include AbbVie (Lupron Depot), Pfizer, Takeda, Sun Pharma, Teva, and Sandoz, operating across North America, Europe, and Asia.

Q2: How does manufacturing complexity affect supply security?
A2: The intricate peptide synthesis process necessitates specialized facilities and expertise, increasing vulnerability to disruptions and emphasizing the importance of diversified manufacturing sources.

Q3: Are biosimilars a significant part of the leuprolide acetate supply chain?
A3: Yes, biosimilars are emerging, especially as patents expire, providing more affordable options and increasing market competition.

Q4: What regulatory factors influence the supply of leuprolide acetate?
A4: Regulatory approval requirements for quality, safety, and efficacy vary by region, impacting manufacturing practices and market access.

Q5: How important is regional manufacturing for global supply?
A5: Regional manufacturing ensures supply continuity, reduces logistics costs, and improves access in emerging markets, making it vital for global coverage.


Sources:
[1] Abbott Laboratories. Lupron Depot Product Information. 2022.
[2] European Medicines Agency. Leuprolide Acetate Summary. 2022.
[3] Takeda Pharmaceutical. Product Portfolio. 2022.
[4] Sun Pharmaceutical Industries. Corporate Reports. 2022.
[5] Market Data Forecast. Pharmaceutical Peptides Market Report. 2022.

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