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info@indeximinternational.com
INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED
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
sam.d@micoson.com
we are Micoson Biopharm Co,.Ltd company from China. We will provide quotation and document support, please send an email to sam.d@micoson.com, we will reply in time. Thank you.
namrata.sutphinrx@gmail.com
Sutphin Drugs Inc are licensed distributors of USFDA approved Reference Listed Drugs (RLD’s) ,Branded & Generic & Comparator Drug Products.
Kindly contact at info@sutphinrld.com or namrata.sutphinrx@gmail.com
tvbbhate@gmail.com
We can support you from a TGA approved site. Do you have the ART no.
You plan to do it on ART L or Rx no.
Let's catch up over email or WhatsApp.
Regards,
Tushar
valueaddedgenerix@gmail.com
+919898263472
lidelong@qrpharma.net
We are a Chinese manufacturer, please contact me
raonk5@gmail.com
Dear Sir,
I can support in giving best formula and process in line with US/EUROPE NDA formula and process and support in preparation dossier. Looking forward for your valuable feedback about this. Need not bother about dossiers which are more theoretical yet times.
Thanking you sir and best regards
Kamalakar Rao N
M.PHARM
INDIVIDUAL CONSULTANT-FORMULATION DEVELOPMENT, DOSSIER SUPPORT & MANUFACTURING
CAN SHARE MY RESUME ONCE RECEIVE YOUR FEED BACK
