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hydrocortisone sodium succinate

Powder and solvent for solution for injection 100 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
United Kingdom
Manufacturer #33720

Established in 1992, this UK-based pharmaceutical manufacturer specializes in the development, manufacturing, marketing, and distribution of a wide range of medicines and supplements. As a CTD dossier owner and manufacturer, it ensures compliance with international quality standards. The company's diverse product portfolio includes categories such as Cold & Cough, Pain Relief (Oral and Non-oral), Antibiotics, Antihypertensives, Antifungals, Anti-malarials, Supplements, Antacids, Anthelmintics, and other therapeutic areas. Operating advanced production lines adhering to stringent GMP guidelines, the manufacturer distributes its products across multiple countries worldwide.

Manufacturer usually replies in 39 days

hydrocortisone sodium succinate

Powder for solution for injection 25 mg, 100 mg, 500 mg, 1000 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #35915

Established in 2007, this family-owned manufacturer specializes in pharmaceutical formulations, offering over 500 products across various dosage forms, including tablets, capsules, dry syrups, ointments, dry injections, and liquid orals. As a CTD dossier owner and manufacturer, it holds WHO-cGMP certification, ensuring compliance with stringent international quality standards. The manufacturer operates advanced production lines with capacities such as 3,600 million tablets, 1,800 million capsules, 240 million liquid injections in ampoules, and 70 million dry powder injections per annum, adhering to rigorous GMP guidelines. As a CTD dossier owner and manufacturer, its products are distributed across multiple countries worldwide.

Manufacturer usually replies in 14 days

hydrocortisone sodium succinate

Powder for solution for injection 100 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #21177

This CTD dossier owner and manufacturer, established in the 1980s, operates within South Asia, specializing in the manufacture and supply of pharmaceutical products. Their offerings include tablets, capsules, eye, ear, and nasal drops, as well as oral and injectable suspensions. The company holds EU and US GMP approvals, signifying adherence to high manufacturing standards. Their production lines cater to a diverse range of therapeutic areas, with a focus on infectious diseases, pain management, and ophthalmology. The company boasts a sizable workforce and has a global reach, catering to markets across the world. They are recognized for their commitment to quality, utilizing high-grade chemicals and advanced machinery for production. The company emphasizes its track record in providing quality pharmaceutical products, underscoring its experience in the industry.

Manufacturer usually replies in 2 days

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