Frequently Asked
Questions
Answers to common questions about our products, licensing, exports and ordering process.
Yes. Therachem Laboratories holds an FDA licence for the manufacture of pharmaceutical products at our facility in Kurla West, Mumbai, India.
Our products are manufactured and tested to meet the standards of I.P., B.P. or U.S.P. as applicable to each product and destination market.
Yes. We export to markets across Africa, Asia and other regions, with full regulatory documentation for destination countries.
We manufacture tablets, capsules, oral suspensions, syrups, oral drops, eye drops and eye ointments.
Possibly. Please contact us with your specific requirements and we will advise whether we can supply or source the product.
Please contact us to discuss your private label or contract manufacturing requirements.
Minimum order quantities vary by product. Please contact us with your requirements for a tailored quotation.
Contact us via the form on this site, by email at therachem@yahoo.com or by telephone at 022-23881886. Include product names, quantities and destination country.
Yes. We provide certificates of analysis, batch documentation and regulatory dossiers as required.
Payment terms are agreed during the order process. Please contact us to discuss your requirements.
Contact our team by email, telephone or via the contact form. We will guide you through pricing, documentation and delivery.
Please contact us for the most up-to-date information on regulatory certifications for specific products.