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diazoxide

Oral suspension 50 mg/ml - 30 ml

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
United States
Unavailable markets
United States
Comments
Reference: Proglycem
Manufacturer #17451

A global specialty-focused pharmaceutical manufacturer that develops and supplies complex pharmaceutical products and active pharmaceutical ingredients, with particular emphasis on hospital, autoimmune, rare-disease and pain-management therapies. The company operates a network of cGMP-compliant facilities that are routinely inspected by major regulators, with at least one manufacturing site holding EU-GMP certification and additional approvals from agencies such as the US FDA, Japanese PMDA and UK authorities, supporting reliable worldwide supply of high-value pharmaceutical products.

diazoxide

Oral suspension 1.5 g/30 ml - 30 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
China
GMP approvals
EU GMP
Manufacturer #34185

Established in 1994, this innovative R&D and manufacturing company focuses on the pharmaceutical and health sectors. As a CTD dossier owner and manufacturer, it ensures compliance with international quality standards, operating sophisticated drug production facilities that meet cGMP specifications from regulatory bodies such as NMPA, FDA, and EMA. The company's diverse portfolio includes biologics, small molecules, synthetic biologics, and special traditional Chinese medicines (TCMs), with over 300 product approvals across various categories. Its products are distributed in more than 40 countries and regions, including Singapore, South Korea, Italy, and China.

diazoxide

Tablets 50 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #10170
A pharmaceutical manufacturer providing export-oriented development and commercial supply of pharmaceutical products across a complete range of finished dosage forms, including tablets, capsules, softgels, injectables, ointments, dry syrups, and sachet presentations. The organisation positions itself as a licensing-and-supply partner with integrated manufacturing expertise and a growing international portfolio, and it reports holding multiple regulatory approvals from major global authorities (including MHRA, TGA, ANVISA and GCC regulators) alongside WHO-GMP compliance for its manufacturing operations, supporting consistent quality and reliability of pharmaceutical products for overseas partners.

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