Suppliers and packagers for BUMEX

BUMEX

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

Applicant	Tradename	Generic Name	Dosage	NDA	NDA/ANDA	Supplier	Package Code	Package	Marketing Start
Validus Pharms	BUMEX	bumetanide	TABLET;ORAL	018225	NDA	Validus Pharmaceuticals LLC	30698-630-01	100 TABLET in 1 BOTTLE (30698-630-01)	1983-02-28
Validus Pharms	BUMEX	bumetanide	TABLET;ORAL	018225	NDA	Validus Pharmaceuticals LLC	30698-631-01	100 TABLET in 1 BOTTLE (30698-631-01)	1983-02-28
Validus Pharms	BUMEX	bumetanide	TABLET;ORAL	018225	NDA	Validus Pharmaceuticals LLC	30698-631-05	500 TABLET in 1 BOTTLE (30698-631-05)	1983-02-28
Validus Pharms	BUMEX	bumetanide	TABLET;ORAL	018225	NDA	Validus Pharmaceuticals LLC	30698-632-01	100 TABLET in 1 BOTTLE (30698-632-01)	1983-02-28
Validus Pharms	BUMEX	bumetanide	TABLET;ORAL	018225	NDA	Validus Pharmaceuticals LLC	30698-632-05	500 TABLET in 1 BOTTLE (30698-632-05)	1983-02-28

Suppliers for the Pharmaceutical Drug: Bumex (Bumetanide)

Last updated: July 29, 2025

Introduction

Bumex, the brand name for bumetanide, is a potent loop diuretic primarily used to treat edema associated with congestive heart failure, liver cirrhosis, and renal disease. Its efficacy hinges on its quality and consistency, making the selection of reliable suppliers critical for pharmaceutical manufacturers, healthcare providers, and distributors. This report comprehensively profiles the primary suppliers of bumetanide, examining their manufacturing capabilities, global reach, regulatory compliance, and strategic positioning within the supply chain.

Global Manufacturing Landscape of Bumex

Bumex is manufactured by several leading pharmaceutical companies known for their robust R&D and manufacturing infrastructure. The primary suppliers encompass both original equipment manufacturers (OEMs) that produce active pharmaceutical ingredients (APIs) and finished drug formulations, as well as contract manufacturing organizations (CMOs). The supply chain is global, with key suppliers based in North America, Europe, and Asia.

Major Suppliers of Bumetanide API

1. Teva Pharmaceuticals

Teva is a pioneering Israeli pharmaceutical firm recognized for producing generic medications, including bumetanide. It maintains extensive manufacturing facilities across Israel, the United States, and Europe.

• Manufacturing Capabilities: Teva produces bumetanide API with cGMP compliance, adhering to stringent quality standards. The company invests heavily in quality control and regulatory compliance, facilitating smooth approval in multiple markets.
• Supply Chain Network: Teva distributes bumetanide through its global network, supplying both APIs and finished drug products.
• Regulatory Standing: Teva’s manufacturing sites are certified by the FDA, EMA, and other regulatory agencies, ensuring the quality and reliability of its products.

2. Novartis

Novartis, a Swiss multinational, manufactures active pharmaceutical ingredients for various therapeutic classes, including diuretics such as bumetanide.

• Manufacturing Capabilities: With state-of-the-art facilities in Switzerland and India, Novartis emphasizes GMP-compliant production of APIs. Their focus on technological innovation ensures high purity and batch-to-batch consistency.
• Global Reach: Novartis supplies bumetanide APIs to several generic companies and hospitals worldwide.
• Regulatory Compliance: Novartis maintains strong regulatory credentials, facilitating market access across regions.

3. Zhejiang Huahai Pharmaceutical Co., Ltd.

A leading Chinese API producer, Zhejiang Huahai supplies bumetanide API for the rapidly growing Asian and global generics markets.

• Manufacturing Capabilities: The company operates large-scale manufacturing sites with robust quality management systems aligned with WHO and GMP standards.
• Market Position: Zhejiang Huahai’s lower-cost API production makes it a significant supplier for generic drug manufacturers in Asia, Eastern Europe, and Latin America.
• Regulatory Standing: While generally compliant, certain regulatory challenges have arisen historically, emphasizing the need for thorough due diligence.

4. Mylan (Now part of Viatris)

Mylan, a major global pharmaceutical company now integrated into Viatris, has a well-established line of generic medications, including bumetanide.

• Manufacturing Capabilities: Mylan's facilities across the U.S., India, and Europe produce high-quality APIs and finished dosage forms.
• Supply Chain: The company's extensive manufacturing and distribution network ensures timely supply for hospitals and pharmacies worldwide.
• Compliance: Mylan maintains certifications from GMP-compliant authorities, ensuring high product standards.

Contract Manufacturing Organizations (CMOs) and Sourcing Options

Several global CMOs facilitate the manufacturing of bumetanide API, offering flexible supply solutions for pharmaceutical firms seeking to outsource production.

• BIONPharma, Inc.: Offers custom API synthesis compliant with international standards.
• CordenPharma: Specializes in active pharmaceutical ingredients with a focus on sterile and non-sterile APIs including diuretics.
• Famar: Operates facilities in Europe, providing API manufacturing with high regulatory standards.

Regulatory and Quality Considerations

Suppliers must adhere to strict regulatory frameworks:

• Good Manufacturing Practices (GMP): Essential for ensuring API consistency, purity, and safety.
• GMP Certifications: FDA, EMA, and WHO certification are indicators of compliance.
• Inspection and Audit Records: Continuous facility audits are critical, especially given past issues with some Chinese API suppliers regarding contamination concerns.

Supply Chain Challenges and Risk Mitigation

• Raw Material Variability: Ensuring stable supply of precursor chemicals is vital.
• Regulatory Divergence: Different markets require varying certifications; suppliers with multi-region approvals offer strategic flexibility.
• Geopolitical Risks: Dependence on certain regions (e.g., China, India) can pose risks; diversification is advisable.
• Supply Disruptions: Pandemic-related disruptions highlight the need for diversified sourcing strategies.

Emerging Trends and the Future of Bumetanide Suppliers

• Shift Toward Diversification: Companies are increasingly diversifying suppliers to reduce reliance on single sources.
• Quality Improvement Initiatives: Suppliers invest in advanced purification and analytical techniques to comply with evolving standards.
• Sustainable Manufacturing: Environmental considerations and corporate responsibility influence supplier assessments.
• Digital Traceability: Enhanced transparency through blockchain and digital tracking to improve supply chain security.

Conclusion

The supply landscape for bumetanide—marketed as Bumex—is characterized by established manufacturers like Teva, Novartis, Zhejiang Huahai, and Mylan. These companies possess the manufacturing expertise, regulatory certifications, and global distribution networks necessary to meet demand reliably. However, supply chain vulnerabilities, regulatory compliance, and geopolitical factors necessitate strategic sourcing, diversification, and rigorous supplier qualification. As demand for affordable diuretics persists, suppliers that can innovate in quality, cost-efficiency, and supply resilience will continue to hold strategic importance.

---

Key Takeaways

• Leading Suppliers: Teva, Novartis, Zhejiang Huahai, and Mylan dominate the bumetanide API supply chain.
• Regulatory Compliance: Manufacturers with certifications from FDA, EMA, and WHO are preferred partners.
• Supply Chain Management: Diversification reduces risk of disruption, especially amid geopolitical and pandemic crises.
• Quality Assurance: Ongoing monitoring and audits ensure API purity and safety, critical in regulated markets.
• Future Outlook: Innovations in manufacturing, digital traceability, and sustainability will influence supplier selection and market dynamics.

---

FAQs

Q1: What are the primary regions where bumetanide suppliers are located?
A1: The dominant regions include North America (mainly the United States and Canada), Europe (notably Switzerland and Germany), and Asia (China and India), with China and India being major low-cost API producers.

Q2: How do quality standards influence supplier selection for bumetanide?
A2: Suppliers with GMP certification and proven regulatory compliance minimize risks related to contamination, efficacy, and safety, ensuring smooth approval processes across markets.

Q3: Are there notable differences between API suppliers in terms of cost and quality?
A3: Yes. Generally, Chinese suppliers offer lower-cost APIs but may face regulatory scrutiny, whereas European and US-based producers often provide higher assurance of quality and regulatory acceptability at a premium.

Q4: What role do contract manufacturing organizations play in the supply of bumetanide?
A4: CMOs provide flexible, scalable manufacturing solutions, enabling pharmaceutical companies to meet demand without investing in extensive in-house infrastructure. They also facilitate access to specialized manufacturing capabilities.

Q5: What emerging trends could impact the future supply of bumetanide?
A5: Trends include increased diversification of suppliers, adoption of digital supply chain technologies, focus on sustainable manufacturing practices, and stricter regulatory standards emphasizing quality and safety.

---

Sources
[1] FDA Orange Book, Pharmaceutical Manufacturer Certifications.
[2] Novartis Official Reports on API Manufacturing.
[3] Zhejiang Huahai Corporate Website and Regulatory Filings.
[4] Teva Pharmaceuticals Annual Reports and Product Approvals.
[5] Industry analysis reports on generic API supply chains.