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stavudine + lamivudine + nevirapine

Tablets 40 mg + 150 mg + 200 mg, 30 mg + 150 mg + 200 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #31070

This pharmaceutical company is a leading global player with over 35 years of experience, operating in more than 60 countries across diverse regions. They specialize in manufacturing a wide range of pharmaceuticals, including prescription medications, over-the-counter drugs, and critical care products. Their extensive portfolio boasts over 350 marketed formulations and 1000+ product registrations, spanning numerous therapeutic areas like oncology, infectious diseases, cardiovascular health, and pain management. The company holds WHO GMP & ISO 9001:2015 certifications, reflecting their commitment to quality and regulatory compliance. Their state-of-the-art manufacturing facility in India utilizes cutting-edge technology and employs a highly skilled workforce dedicated to delivering affordable, high-quality products.

Manufacturer usually replies in 84 days

stavudine

Capsules 30 mg, 40 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
GMP, WHO
Manufacturer #24869

This CTD dossier owner and manufacturer, established over three decades ago in South Asia, has become a prominent player in the global pharmaceutical market. Their focus lies in manufacturing and exporting a wide array of pharmaceutical products, including prescription and over-the-counter medications, to regulated and non-regulated markets worldwide. They have a strong presence in regions like Latin America, the Middle East, CIS, and Asia, with a subsidiary established in the Caucasus. Their commitment to quality is evident through adherence to WHO GMP standards, along with EU and USFDA guidelines. They specialize in manufacturing solid dosage forms and have a diverse range of therapeutic areas, although specific details were not provided.

Manufacturer usually replies in 78 days

stavudine

Oral suspension 1 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20401
This pharmaceutical company has two decades of experience manufacturing cost-effective medications across various therapeutic areas. Their product portfolio includes tablets, capsules, injectables, liquid orals, and topical solutions. They specialize in expert formulation development and possess advanced analytical capabilities to ensure quality and regulatory compliance. The company's key markets include the EU and North America. Their GMP certified manufacturing facility is strategically located near a major commercial hub.

Manufacturer usually replies in 21 days

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