29 Jan 2021

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Pidotimod Finished Dosage Formulations needed in Vietnam [ENA09603]
Ha Dong Pharmaceutical, a company that trades in cosmetics, sanitary products, nutritional foods and functional foods is looking for suppliers of Pidotimod Finished Dosage Formulations of various dosage forms. The required quantity for the first year is 2,000 units, the second year is 3,000,000 units and the third year is 5,000,000 units. The suppliers must support this enquiry with Dossier for Zone IVB according to ACTD and GMP. European suppliers are preferred. Interested suppliers can contact them via their email: lee@hadongpharm.com.
1. Pidotimod (800 mg) Granules per Oral Solution
2. Pidotimod (400 mg) Vials
3. Pidotimod (400 mg) Tablets

Comments :

info@indeximinternational.com

Indexim international, are one of the leading supplier, exporter and importer of Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard,, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements. Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian countries 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.

Indexim International
sales.indeximinternational@gmail.com
info@indeximinternational.com
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407

15:13,  29 Jan 2021

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

23:30,  29 Jan 2021

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

23:30,  29 Jan 2021

bdvizag@leepharma.com

We are the EU GMP, WHO GMP Certified manufacturer of Finished dosage form.

We are open for product registration,with ACTD Dossier.

Kindly let us know your interest.

Best regards
bdvizag@leepharma.com

16:26,  02 Feb 2021

info@sutphinrld.com

Sutphin Drugs Inc are licensed distributors of USFDA approved RLD’s,(Branded & Generic) Drug Products including controlled (Narcotic / Psychotropic) products sold in the United States

Kindly contact at info@sutphinrld.com or sutphinrx@gmail.com

20:08,  16 Feb 2021

vvarma@zeonhealth.com

Dear Sir/Madam




Zeon Groups provide you from  GMP Certified Mfg plant   with high-quality APIs, Semi finish formulation and herbal and phytochemicals API at competitive prices,  while meeting the most stringent
 industry standards. Our products have been known for its quality, reliability and affordability. 


Minoxidil 
Minoxidil 
sulphate
Gabapentin
Gliclazide
Rosvastatin calcium
Loratidine 
Levocetrizine dihcl
Pioglitazole
Iran sucrose
Ketoconzole
Clotrimazole 
Miconazole nitrate
Molnupiravir
Favipiravir
Colchcine usp
Thiocolchicoside
Serratiopetidase 
Bromelin
Omeprazole pellets 
Telmisartan dc granules 
Naproxen sodium dc granules


We believe  our success based on customer satisfaction. Kindly email us directly for the confirmation of your requirement so we can share the Quotation, COA along with the others information 
 within 24hrs Max from the inquiry date;


You may also reach us through this number (Call/WhatsApp) on +9821702300 or Skype :
zeonpharmaindia@hotmail.com




Regards
Vinod Varma
Managing partner
Zeon health Industris
Zeon drugs Pvt ltd
sales@zeondrugs.com ,
vvarma@zeonhealth.com
Whatapp/ call :+919821702300

07:00,  03 Sep 2021
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