Suppliers and packagers for modafinil

modafinil

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

Applicant	Tradename	Generic Name	Dosage	NDA	NDA/ANDA	Supplier	Package Code	Package	Marketing Start
Alembic	MODAFINIL	modafinil	TABLET;ORAL	202700	ANDA	Alembic Pharmaceuticals Limited	46708-385-10	100 TABLET in 1 CARTON (46708-385-10)	2017-06-30
Alembic	MODAFINIL	modafinil	TABLET;ORAL	202700	ANDA	Alembic Pharmaceuticals Limited	46708-385-30	30 TABLET in 1 BOTTLE (46708-385-30)	2017-06-30
Alembic	MODAFINIL	modafinil	TABLET;ORAL	202700	ANDA	Alembic Pharmaceuticals Limited	46708-385-60	60 TABLET in 1 BOTTLE (46708-385-60)	2017-06-30
Alembic	MODAFINIL	modafinil	TABLET;ORAL	202700	ANDA	Alembic Pharmaceuticals Limited	46708-385-90	90 TABLET in 1 BOTTLE (46708-385-90)	2017-06-30

Suppliers for the Pharmaceutical Drug: Modafinil

Last updated: July 27, 2025

Introduction

Modafinil is a widely prescribed wakefulness-promoting agent primarily used for conditions such as narcolepsy, shift work sleep disorder, and excessive daytime sleepiness associated with obstructive sleep apnea. As a Schedule IV controlled substance in many jurisdictions, the drug’s manufacturing, distribution, and supply chain are tightly regulated to ensure compliance with safety and quality standards. Understanding the key suppliers in the global Modafinil market provides critical insights for pharmaceutical companies, healthcare providers, and regulatory bodies seeking to navigate this complex landscape.

Global Manufacturing Landscape of Modafinil

The supply chain of Modafinil is predominantly composed of generic pharmaceutical manufacturers and some original patent holders. While the original formulation was developed by Cephalon (now part of Teva Pharmaceuticals), the entry of generic manufacturers has expanded globally, resulting in a diversified supplier base. This proliferation is particularly apparent in regions with robust pharmaceutical manufacturing capabilities, such as India, China, and Eastern Europe.

Original Manufacturer

Cephalon (Teva Pharmaceuticals)
Cephalon originally developed Modafinil under the brand name Provigil in the late 1990s. After its acquisition by Teva Pharmaceuticals, the patent protections for Provigil expired, paving the way for generic manufacturers to enter the market. Teva remains a significant source of high-quality Modafinil, especially for branded formulations, although it has faced generic competition.

Major Generic Suppliers

Following patent expiration, numerous generic manufacturers have emerged, especially in countries with significant pharmaceutical manufacturing infrastructure:

1. Hetero Drugs (India)
   An established producer of generic pharmaceuticals, Hetero supplies bulk Modafinil to various markets globally. Their facilities are compliant with WHO-GMP standards, ensuring product quality.

2. Sun Pharmaceutical Industries (India)
   As India’s largest pharmaceutical company, Sun Pharma produces generic Modafinil and exports to multiple regions. Their manufacturing facilities adhere to strict regulatory standards, including USFDA compliance.

3. Dr. Reddy's Laboratories (India)
   Dr. Reddy’s is recognized for its rigorous quality standards and extensive distribution network, supplying high-quality Modafinil globally.

4. Mylan (now part of Viatris)
   Mylan is a significant player in the generic pharmaceutical space, with production facilities compliant with international quality standards, including for Modafinil.

5. Sichuan Taiji Pharmaceutical (China)
   Specializing in off-patent pharmaceuticals, this Chinese manufacturer supplies generic Modafinil primarily to Asian markets.

6. Intas Pharmaceuticals (India)
   With a reputation for quality generics, Intas supplies Modafinil to various global markets.

Emerging and Niche Suppliers

Several smaller or regional manufacturers produce Modafinil primarily for local markets or as intermediaries. The diversity of suppliers often depends on regional regulatory approvals, quality certifications, and export licenses.

Regulatory and Quality Considerations

Given the controlled status of Modafinil, suppliers must comply with rigorous GMP standards and obtain relevant approvals from authorities like the US Food and Drug Administration (FDA), European Medicines Agency (EMA), or local regulators such as India’s Drug Controller General (DCGI).

Many suppliers are equipped with certifications such as:

• USFDA approval for manufacturing facilities
• European GMP certification
• ISO certifications for quality management

The integrity of supply chains can be compromised by the proliferation of unregulated or counterfeit sources, especially in online markets, underscoring the importance of sourcing from reputable and certified suppliers.

Supply Chain Challenges

• Regulatory hurdles: Different jurisdictions have varying approval processes which can delay or restrict the import and distribution of Modafinil.
• Patent and legal issues: Although many patents have expired, legal disputes can impact supply continuity.
• Counterfeit products: The high demand for Modafinil has led to an influx of counterfeit or substandard products, particularly in unregulated online markets.
• Supply disruptions: Raw material shortages, manufacturing issues, or regulatory sanctions can cause supply interruptions.

Market Dynamics and Competitive Strategies

Leading suppliers compete based on:

• Product quality and compliance standards
• Pricing and market penetration strategies
• Supply chain reliability
• Regulatory approval and certifications

Companies investing in Good Manufacturing Practice (GMP) certification and robust quality assurance processes tend to secure preferred supplier status among healthcare providers and distributors.

Future Outlook

The global Modafinil market is expected to sustain growth, driven by expanding indications and increasing acceptance across various medical and off-label uses. Suppliers investing in quality assurance, regulatory compliance, and supply chain resilience will be better positioned to capitalize on this growth.

Emerging markets such as Southeast Asia, Latin America, and Africa will continue to attract generic manufacturers, leading to diversification in the supplier landscape. Additionally, advancements in synthetic manufacturing processes may lower production costs, potentially impacting supplier pricing strategies.

Key Takeaways

• The Modafinil supply chain is dominated by Indian and Chinese generic manufacturers, with key players including Hetero Drugs, Sun Pharma, Dr. Reddy’s, Mylan, and Sichuan Taiji.
• Original patent holders such as Teva Pharmaceuticals now primarily produce branded formulations but face intense competition from generics.
• Strict regulatory standards, including GMP compliance and international certifications, are crucial for market access and supply security.
• Market growth trends favor suppliers who can ensure consistent quality and reliable distribution channels amidst regulatory and counterfeiting challenges.
• Geographic diversification offers opportunities but also necessitates rigorous compliance and quality controls to mitigate risks.

FAQs

1. Which countries are the leading suppliers of Modafinil globally?
India and China are the primary sources of generic Modafinil, with significant manufacturing capacities contributing to global supply. European and North American markets rely more on imports from these regions due to regulatory approvals.

2. Are there legal risks associated with sourcing Modafinil from unregulated suppliers?
Yes. Unregulated suppliers often produce counterfeit or substandard products, risking legal penalties, health risks, and damage to reputation. It's essential to verify supplier certifications and regulatory compliance.

3. How can companies ensure the quality of Modafinil from international suppliers?
By sourcing from manufacturers with established GMP certifications, comprehensive quality assurance processes, and regulatory approvals such as USFDA or EMA certifications.

4. Will the market for Modafinil remain competitive?
Yes. Market expansion into new therapeutic and off-label applications, coupled with increased manufacturing capacity, is likely to intensify competition among established and emerging suppliers.

5. What are the implications of patent expirations for Modafinil suppliers?
Patent expirations have facilitated the entry of numerous generics, expanding supply options but also increasing price competition and market saturation.

References

1. [1] U.S. Food and Drug Administration (FDA). Approved Drug Products with Therapeutic Equivalence Evaluations. https://www.fda.gov
2. [2] World Health Organization. WHO Good Manufacturing Practices (GMP) guidelines.
3. [3] Teva Pharmaceuticals. History of Modafinil and Provigil.
4. [4] Market research reports on the global generic pharmaceutical industry.
5. [5] Regulatory bodies’ databases and approval listings for pharmaceutical manufacturing sites.

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Prepared by: Expert Pharmaceutical Patent Analyst
Date: March 2023