04 Mar 2021

Reply

Penicillin G Sodium (1.3 MT) API needed in Belgium [ENA09872]
A company that deals in pharmaceuticals and nutritional supplements is looking for suppliers of Penicillin G Sodium (CAS 69-57-8) API for commercial purposes. The required quantity is 1.3 MT. The suppliers must support this enquiry with EU GMP and DMF.

Comments :

info@indeximinternational.com

Indexim international, one of the leading suppliers, 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

16:41,  04 Mar 2021

sam.d@micoson.com

we would like to participate in the quotation and provide documentary support. Please send an email to sam.d@micoson.com. We will reply to the quotation within 7 hours,
Thank you for your support.

16:45,  04 Mar 2021

shen.li.mo@vladachem.com

Dear Sir/Miss,

We would like to offer you the quotation. Please send an email to us for more detail of your inquiry. Thank you.

info@vladachem.com
www.vladachem.com

Best Regards,

17:37,  04 Mar 2021

Greetings of the day sir,

we are siyahi traders from Tamilnadu, India. Who supply all kinds of active pharmaceutical ingredients world wide. Got your mail through market place.

I came to know that you are interested in purchasing Penicillin G Sodium. Our products HSN quality is 99.99% which you can test by availing some sample.

For Price and details plz Kindly reach us at mohitha.shenba18@gmail.com or by mobile +917010080177.

Thank you,
Siyahi traders.

11:44,  05 Mar 2021

alicechan@huarizy.com

HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.

1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80

email address: alicechan@huarizy.com
phone number: +86 18820220687

11:47,  05 Mar 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

00:55,  06 Mar 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

00:56,  06 Mar 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

00:56,  06 Mar 2021

mroverseasbd03@gmail.com

Please email us your inquiry with quantity. We are a leading international indenting agent. We have good reliable sources. please send us mroverseasbd03@gmail.com

10:53,  06 Mar 2021

aykutdikenli@in-pharm.de

Dear Sir / Madam,

I`d like to introduce myself/my company shortly.

I can look back to more than 20 years of experience as procurement/sales manager, BD manager ie. independent mediator/consultant for API`s.

I was working for a German trading company in Hamburg from 2001 – 31.12.2019.
With effect of 01.01.2020, I do run my own company ie. IN-PHARM, located in Hamburg, Germany.

I work with many leading end-users mainly located in Turkey, Greece, Romania. They consider me as their prolonged arm for sourcing activities.

Optimize your sourcing activities for commercially available generic API s.
Get an extraordinary fast and uncomplicated access to all API`s and professional, documentary holding manufacturers from a single company, namely IN-PHARM, located in Hamburg, Germany.

All who likes to have below mentioned advantages should use IN-PHARM:

- A fast access to all commercially available generic API`s and manufacturers worldwide
- Independent consultant who provides advantageous prices
- Provision of documentation needed for MA application purposes on regulated markets
- Professionalism, flexibility, full transparency and sustainable and excellent pre & after-sales service

I would be more than glad to support you during your API sourcing activities. It may be for new RD´s and/or manufacturer alteration projects.
You will get all data/information you need under one roof and that unusually fast.

Your inquiries are highly welcome !

Best regards / Selamlar

Aykut Dikenli
IN-PHARM

Tel.: +49-40-739 5477
Mobile: +49-179-815 8864
E-Mail: aykutdikenli@in-pharm.de

IN-PHARM
Inh. Aykut Dikenli
Bockhorster Höhe 190
D-21031 Hamburg
Germany
VAT: DE328462565

16:20,  09 Mar 2021

jgq@yangzijiang.com

jgq@yangzijiang.com

I am Justin from Yangtze River Pharmaceutical Group in China

APIs and FDF can be manufactured by our company.

We can also CMO

If you need them, please contact me by Tel., WhatsApp and Wechat: +86 15261051195
Email: jgq@yangzijiang.com

17:28,  09 Mar 2021

zhang.chunlin@reyoungh.com

This is Reyoung PHARAM from China ,
We are factory,
we can offer and give best price ,
Please email me

05:48,  11 Mar 2021
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