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Isavuconazole manufacturers

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isavuconazole

Capsules 100 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
Iceland
GMP approvals
EU GMP
Manufacturer #28915

This company specializes in generic pharmaceuticals within the EU region. They offer out-licensing and contract manufacturing services to pharmaceutical companies seeking high-quality production from a reliable European partner. Their facility utilizes green energy sources, highlighting their commitment to sustainability. While specific therapy areas and product details are not provided, they likely focus on various dosage forms common in generic pharmaceuticals. The company emphasizes its skilled workforce and dedication to employee well-being.

Manufacturer usually replies in 23 days

isavuconazole

Solution for injection 200 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Unavailable markets
Estonia , Latvia , Lithuania
Manufacturer #2346
This pharmaceutical company, based in Europe, has a track record spanning several decades. They offer a diverse product portfolio, including prescription and over-the-counter medications, mainly in solid and liquid dosage forms. They are particularly known for their expertise in lyophilized products. The company has achieved global reach through licensing, exports, and third-party manufacturing agreements, with a strong presence in Europe, North America, and emerging markets in the Middle East, Latin America, and Asia Pacific. Their manufacturing facilities adhere to strict European and international Good Manufacturing Practices (GMP) standards. Key focus areas include generic pharmaceuticals and technology transfer services for third-party products.

Manufacturer usually replies in 21 days

isavuconazole

Injection 200 mg

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
China
GMP approvals
FDA
Unavailable markets
United States
Manufacturer #38346
Manufacturer was incorporated on 27 December 2021 in Surat, Gujarat, India, with about 28 employees. As a CTD dossier owner and manufacturer, it operates a WHO-GMP certified and EU-compliant formulation plant under CGMP norms. Products reach markets in India, Yemen, Zambia, Venezuela, Ghana, Kenya, and Tanzania for international presence. Designed to comply with rigorous “Revised Schedule M” rules from India’s Drug Controller. As a CTD dossier owner and manufacturer, it aims for regulatory readiness in global submissions. Recognized as a GMP manufacturer, it ensures standards of safety, purity, and efficacy in all batches.

Manufacturer usually replies in 9 days

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