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etofylline + theophylline

Injection 84.7 mg + 25.3 mg - 2 ml

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 7 days

etofylline + theophylline

Solution for injection 2 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #2303
A pharmaceutical manufacturer with over 25 years of experience that develops and produces fixed-dose and single-entity generic and specialty pharmaceutical products. The company offers an extensive range of injectable dosage forms, including parenterals, and also manufactures oral solids. Its facilities operate under recognised international quality certifications such as EU-GMP, ANVISA, PIC/S and TGA approvals, supporting reliable large-scale production of pharmaceutical products for global export while emphasizing efficacy, affordability and consistent quality.

Manufacturer usually replies in 21 days

etofylline + theophylline

Injection 84.7 mg + 25.3 mg/ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #34549

Established in 2016, this WHO-GMP certified manufacturer specializes in the production and export of pharmaceutical, nutraceutical, and ayurvedic products, including tablets, capsules, syrups, and injections. As a CTD dossier owner and manufacturer, it ensures compliance with international quality standards. The company operates state-of-the-art manufacturing facilities adhering to stringent GMP guidelines. Its products are distributed across multiple countries worldwide, with registrations in regions such as the Dominican Republic, Philippines, Myanmar, Uzbekistan, Turkmenistan, Iraq, and Kuwait. 

 

Manufacturer usually replies in 14 days

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