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megestrol

Tablets 160 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
EU GMP
Comments
Ref: Megace ®
Manufacturer #337
A pharmaceutical manufacturer based in the EU that has been active in 90+ countries selling its products in the EU, Africa, North America, Middle East, and Asia for 30+ years. Key production lines are Rx and OTC. Main therapeutic areas include diabetes, CNS, and dermatology. The company's production lines are GMP-compliant. The company possesses branches in the Middle East and Asia.

Manufacturer usually replies in 17 days

megestrol

Tablets 40 mg, 160 mg

Dossier type
CTD
Dossier status
Under development
Country of origin
India
GMP approvals
EU GMP
Manufacturer #15176
A sterile-focused pharmaceutical manufacturer specialising in the development and commercial supply of liquid and lyophilised injectable pharmaceutical products in vials and ampoules. Its advanced manufacturing facility is described as compliant with international regulatory agencies, and the company highlights cGMP approvals and renewals from authorities such as the US FDA, UK MHRA, ANVISA, INVIMA and EU GMP bodies, supporting high-volume capacity and reliable global supply of injectable pharmaceutical products.

Manufacturer usually replies in 57 days

megestrol

Tablets 40 mg

Dossier type
ACTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
India
Manufacturer #18530

This pharmaceutical company specializes in a diverse range of products including prescription medications, over-the-counter drugs, medical devices, and supplements. They hold WHO-GMP certifications since 1965 and an ISO 9001:2015 certification, demonstrating their commitment to quality. Their expertise spans various therapy areas such as oncology/hormone therapies, cardiovascular health, and gastrointestinal conditions. They offer a wide range of dosage forms including capsules, tablets, syrups, and rectal suspensions. This company has a global presence, with products distributed across over 2000 countries. They are known for their contract manufacturing capabilities and new drug development expertise, holding over 300 ACTD dossiers.

Manufacturer usually replies in 14 days

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