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1. Tramadol (75 mg) + Dexketoprofen (25 mg) Film Coated Tablets. The required quantity is 30,000 packs for first year & 105,000 packs for fifth year of 10 units.
2. Tramadol (75 mg) + Dexketoprofen (25 mg) Film Coated Tablets. The required quantity is 60,000 packs for first year & 140,000 packs for fifth year of 15 units.
3. Tramadol (75 mg) + Dexketoprofen (25 mg) Film Coated Tablets. The required quantity is 190,000 packs for first year & 410,000 packs for fifth year of 20 units.
info@eqpharma.com
please contact us.we can help
info@aeqpharma.com
We can hel you on EUCTDs
vishvesh.shaishav@gmail.com
We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.?We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.?Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates ?Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.?vishvesh.shaishav@gmail.com
+919725487108
+919726387108
export1@pranadabiopharma.com
Hello! Greetings from Pranada Biopharma Pvt. Ltd. We can supply your required Product at the best rate. Please contact us at export1@pranadabiopharma.com for more details.
Sales@mishupharma.com
Dear Sir/ Madam,
We are a supplier based in India. We can provide you APIs intermediates, columns, excipients, EP/BP/USP/Inhouse standards at a very good price and quality.
Please let us know if you have any requirements from India.
Looking forward to hearing from your end.
vishvesh.shaishav@gmail.com
We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.?We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.?Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates ?Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.?vishvesh.shaishav@gmail.com
+919725487108
+919726387108
info@setarehsalian.com
Subject: Tramadol 50 mg and 100 mg Supply Inquiry Response
Dear Sir/Madam,
Setareh Salian Company can fulfill your requirements for Tramadol 50 mg and 100 mg tablets. We collaborate with GMP-compliant manufacturers in Iran. Let us know your quantity needs for competitive pricing and timely delivery.
Best Regards,
Arian Esmaeili
Sales Manager
Setareh Salian Company
Email: info@setarehsalian.com
Phone: +989360015000
