28 Nov 2024

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Sitagliptin (5 kg) API needed in Egypt [ENA21249]
A company that focuses on manufacturing of various finished formulations is looking for suppliers of USP/ BP Grade Sitagliptin (5 kg) API for development purposes. The suppliers must support this enquiry with DMF, GMP & CoA.

Comments :

foramjjani@gmail.com

Hello,
I am Foram from India. I provide assistance for regulatory & QA documents like DMF, dossier, PV, AMV etc. Whtsapp: +919819435009

19:54,  28 Nov 2024

scisearch@menovopharm.com

Dear, sir/ madam.

Menovo Pharmaceutical is prepared to supply Sitagliptin API, adhering to stringent quality standards and regulatory compliance. We value your consideration of this offering and anticipate the opportunity to explore potential collaboration avenues that could benefit both parties.
China.
Marri venkateswarlu
scisearch@menovopharm.com
+ 86 13586278474.

09:01,  29 Nov 2024

olga.igumnova@zspcompounds.com

Zhejiang Syntech Pharm, a trustfull provider of high-quality API (incl.Sitagliptin), Intermediates and solutions.
Through our well-established network of partners, we can offer you a diverse range of pharmaceutical ingredients catering to various therapeutic areas, including but not limited to:
Active Pharmaceutical Ingredients (APIs): Our API produced by top Chinese manufactuers which mostly certified by NMPA and partly certified by FDA/EDQM/PMDA etc.

11:48,  29 Nov 2024

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, liposomal iron,Intermediates, , 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 APPROVE

12:31,  29 Nov 2024

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

22:41,  29 Nov 2024

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

22:41,  29 Nov 2024

sgs@hrvglobal.com

Dear Sir/Madam,

We understood that you have requirement for Sitagliptin and we can supply to your esteemed company.

HRV Global is in API Business supplying to Global Regulated markets with our Own Manufacturing and distribution portfolio.
The APIs are manufactured in FDA & EUGMP Inspected and approved Sites and as well as accredited by various global regulatory
authorities. We are a market expansion company and representing 50+ Indian API makers & their 400+ API portfolio
in Global market.

11:00,  02 Dec 2024

S.arab@parsianpharma.com

Dear,Hope this message finds you well.
We are a well known API Manufacturer with 6 GMP Licensed dedicated production lines for both API & Granule.
we can supply you Sitagliptin API with USP Specification.

12:14,  04 Dec 2024

sales@mishupharma.com

Hi,
We can supply the same with US DMF. Send your complete query by email.

16:28,  06 Dec 2024
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