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Country of origin : India

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sulfadoxine + pyrimethamine

Tablets 500 mg + 25 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #20386

This pharmaceutical manufacturing company boasts over four decades of experience in producing and marketing a wide range of products across various therapeutic areas. Specializing in general tablets, hormonal tablets, and oral powders, they cater to markets in both the domestic and international sphere. Their key therapy areas include gastrointestinal disorders, cardiovascular health, urology, allergy treatment, contraception, and hormone replacement therapy. With a focus on quality and cost-effectiveness, they provide comprehensive service support to a loyal customer base spanning regions like North America and the EU.

Manufacturer usually replies in 9 days

pyrimethamine + sulfadiazine

Tablets 500 mg+25 mg

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
FDA
Manufacturer #19316
This pharmaceutical company specializes in both over-the-counter (OTC) and prescription generic drugs, offering products in the form of tablets, capsules, and liquids. Founded in 1992, they initially focused on the US market before expanding globally. They hold a significant distinction as the first Indian company to receive USFDA approvals for producing both OTC and prescription drugs for the US market. Their manufacturing facility is located in India, with a dedicated marketing and distribution center in the USA. Key therapy areas are not specified, nor are details about specific product patents or GMP certifications provided.

Manufacturer usually replies in 19 days

pyrimethamine

Tablets 25 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #10170
A pharmaceutical manufacturer providing export-oriented development and commercial supply of pharmaceutical products across a complete range of finished dosage forms, including tablets, capsules, softgels, injectables, ointments, dry syrups, and sachet presentations. The organisation positions itself as a licensing-and-supply partner with integrated manufacturing expertise and a growing international portfolio, and it reports holding multiple regulatory approvals from major global authorities (including MHRA, TGA, ANVISA and GCC regulators) alongside WHO-GMP compliance for its manufacturing operations, supporting consistent quality and reliability of pharmaceutical products for overseas partners.

Manufacturer usually replies in 29 days

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