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Dexibuprofen manufacturers

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Country of origin : South-korea

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18 products found

dexibuprofen

Tablets 400 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
South Korea
GMP approvals
PICS
Manufacturer #18082
The company was formed in the 1970s with a management philosophy leaving an immortal corporate image to protect human life from diseases. They are trying to strengthen as specialized in manufacturing generic medicines. They are growing continuously and the drug was continuously known for its excellence all over the world, exporting natural herb medicine and generic drug to china and Southeast Asia area.

Manufacturer usually replies in 8 days

dexibuprofen

Tablets 400 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
South Korea
GMP approvals
PICS
Manufacturer #35087

Established in 2020, this manufacturer employs approximately 677 individuals and specializes in providing comprehensive pharmaceutical manufacturing services, including product development, analytical and regulatory services, as well as clinical and commercial manufacturing and packaging for various dosage forms. As a CTD dossier owner and manufacturer, it holds GMP certifications from international regulatory authorities, ensuring compliance with stringent quality standards. The manufacturer operates advanced production lines adhering to rigorous GMP guidelines. As a CTD dossier owner and manufacturer, its products are distributed in over 20 countries worldwide.

Manufacturer usually replies in 14 days

dexibuprofen

Tablets 300 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
South Korea
GMP approvals
PICS
Manufacturer #20956

Established in 1987, this Manufacturer is a CTD dossier owner and manufacturer with a global footprint spanning over 42 countries and regions. With approximately 665 employees, it operates GMP-certified facilities in South Korea, producing tablets, capsules, and injectable formulations. As a GMP manufacturer, it holds certifications such as PIC/S GMP, EU GMP, and FDA 21 CFR compliance. The Manufacturer's commitment to excellence as a CTD dossier owner and manufacturer and GMP manufacturer solidifies its reputation in the global pharmaceutical market

Manufacturer usually replies in 26 days

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