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Etomidate manufacturers

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Country of origin : India

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5 products found

etomidate

Injection 20 mg/10 ml

Dossier type
EU CTD
Dossier status
Under development
Country of origin
India
GMP approvals
EU GMP
Manufacturer #19912

This global pharmaceutical company is a leading manufacturer of specialty formulations in oncology and anesthesia, with operations spanning the EU, North America, and other regions. They specialize in prescription medications, including lyophilized products, for key therapy areas such as cancer treatment and pain management. Their commitment to quality is reflected in their numerous GMP certifications, including WHO GMP, EU GMP, and TGA certifications. They prioritize innovation through research and development of new manufacturing processes and drug delivery mechanisms.

Manufacturer usually replies in 37 days

etomidate

Vials, injection 2 mg/ml - 10 ml, 20 ml

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
FDA
Comments
ANDA / R &D Status: Approved ; US RLD / Holder: "Amidate / Hospira"; Indication: General Anaesthetic;
Manufacturer #8216
This fast-growing pharmaceutical company boasts a dominant presence in Latin America, Francophone Africa, and a growing footprint in regulated markets like the EU and North America. Founded in 1990, it initially focused on ointments and creams before expanding its product range significantly. With over 4,000 global product licenses, they cater primarily to the "Bottom of the Pyramid" through their owned distribution networks. The company's manufacturing facility holds multiple certifications including US FDA approval (with three successful inspections since 2016), EU-GMP, ANVISA-Brazil, INVIMA-Colombia, and COFEPRIS-Mexico. They prioritize innovation with a significant portion of their earnings invested in research and development of safe and effective products across various dosage forms. Key therapy areas are not specified.

etomidate

Vials 2 mg/ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #33693

Established in 2013, this manufacturer specializes in producing high-quality generic formulations in the oncology and hormonal segments. As a CTD dossier owner and manufacturer, it adheres to strict GMP guidelines, ensuring its products meet rigorous international standards. The manufacturer operates cutting-edge production facilities that are designed to meet the demands of global markets. As a CTD dossier owner and manufacturer, it distributes its products across various countries, reinforcing its commitment to enhancing patient care globally.

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