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Country of origin : India

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metoclopramide hydrochloride

Tablets 5 mg, 10 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Registered in
Australia , New Zealand
Available for
Licensing with supply, Distribution only
Manufacturer #638

A pharmaceutical manufacturer producing a broad range of pharmaceutical products that include finished dosage forms such as tablets, capsules, oral liquids and other formulations for various therapeutic areas, as well as active pharmaceutical ingredients used in drug manufacture and export to global markets. The company integrates research and development with large-scale production and maintains quality systems aligned with industry standards to support safety, consistency and compliance in the development and supply of its pharmaceutical products.

Manufacturer usually replies in 95 days

metoclopramide hydrochloride

Tablets 5 mg, 10 mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #11548
This pharmaceutical company is a global leader in research, development, manufacturing, and regulatory support for a wide range of products. They offer end-to-end services, from initial product identification to commercialization, catering to the healthcare needs of over 29 countries across multiple regions including North America, Europe, Asia, and Africa. Their expertise spans various therapeutic areas such as anti-infectives, CNS disorders, gynecology, allergy treatment, erectile dysfunction, and gastrointestinal conditions. They utilize diverse dosage forms like oral solids, topicals, and liquids, with packaging options tailored to each product. The company holds significant GMP certifications from international regulatory bodies, ensuring the quality and safety of their products. Their dedicated team of scientists continuously drives innovation and development within their certified research facility.

Manufacturer usually replies in 16 days

metoclopramide hydrochloride

Tablets 5 mg, 10 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #31580

Established in 1990, this Indian manufacturer employs approximately 3,065 individuals and specializes in developing and manufacturing IP-led niche finished dosage formulations. As a CTD dossier owner and manufacturer, it holds GMP certifications from major regulatory authorities, including the US FDA, EU-GMP, Health Canada, and UK MHRA, ensuring compliance with stringent international quality standards. The company operates eight manufacturing units across India, Singapore, Italy, the United States, and Kenya, producing a range of products, including soft gelatin capsules, tablets, and ointments. As a CTD dossier owner and manufacturer, its products are distributed in over 100 countries worldwide.

Manufacturer usually replies in 35 days

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