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Country of origin : India
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trimetazidine dihydrochloride

Tablets 20 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP, TGA
Manufacturer #18120
This globally competitive organization specializes in formulating a wide range of medications and exports to over 40 countries. Their state-of-the-art manufacturing facilities are strategically located across three cities, adhering to stringent regulatory standards like those set by the EU, UK, and UNICEF. They produce diverse dosage forms including tablets, capsules, creams, ointments, gels, and sterile formulations such as lyophilized products and prefilled syringes. Key therapy areas include complex generics, orphan drugs, and treatments for neglected tropical diseases. The company holds GMP certifications and possesses product patents, emphasizing their commitment to quality and innovation. They actively participate in global initiatives, providing emergency stockpiles for coronavirus treatments and partnering with organizations to address the healthcare needs of Palestinian refugees.

Manufacturer usually replies in 42 days

trimetazidine dihydrochloride

Tablets, extended release (ER) 35mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
India
Manufacturer #557

This organization is a multinational pharmaceutical company dedicated to providing affordable healthcare globally. They offer over 1,500 products across various therapeutic areas including HIV/AIDS, making significant contributions to accessibility in emerging markets like India, South Africa, and the U.S. Their product portfolio encompasses over 50 dosage forms, ranging from prescription medications and OTC drugs to potentially medical devices and supplements. They prioritize GMP certifications and hold patents for key products. Their commitment to affordability and inclusiveness has earned them recognition as a leader in global health initiatives.

Manufacturer usually replies in 35 days

trimetazidine dihydrochloride

Tablets 20 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20400

This company is a leading manufacturer of generic APIs and intermediates with over 30 years of experience in the pharmaceutical industry. They offer a wide range of products, including Azithromycin and Erythromycin, serving global markets from three manufacturing facilities. The company prioritizes research and development to continuously improve processes and product offerings. They hold WHO-GMP certifications and adhere to stringent quality standards (cGMP) across all their operations. While they specialize in APIs and intermediates, they also provide contract manufacturing services for innovators and large pharmaceutical companies. Their expertise spans multiple therapy areas, with a focus on key dosage forms like tablets and capsules.

Manufacturer usually replies in 60 days

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