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1. Pemetrexed Disodium (110.29 mg and 551.43 mg) Ampoules. The required quantity is 47 units and 55 units respectively.
2. Carboplatin (450 mg and 150 mg) Ampoules. The required quantity is 57 units and 75 units respectively.
3. Cisplatin (50 mg) Ampoules. The required quantity is 32 units.
4. Docetaxel (20 mg and 80 mg) Ampoules. The required quantity is 20 units and 41 units respectively.
5. Fluorouracil (1 MT and 5 MT) Ampoules. The required quantity is 144 units and 63 units respectively.
6. Doxorubicin Hydrochloride (50 mg) Concentrated Solution. The required quantity is 11 units.
7. Etoposide (100 mg) Ampoules. The required quantity is 180 units.
8. Oxaliplatin (100 mg) Concentrated Solution. The required quantity is 92 units.
9. Topotecan Hydrochloride (1.09 mg and 4.35 mg ) Concentrated Solution. The required quantity is 53 units and 14 units respectively.
10. Calcium Folinate (1080.39 mg) Solution for Infusion. The required quantity is 89 units.
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 various finished dosage formulations. 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.
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
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
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
export@healthpharma.in
Dear Sir,
Greetings from Health Pharma...!!!
We can support you with your requirements. Kindly request you to send email for detailed information.
Looking forward to your positive response.
Thanks...!!!
jeffery@holypharm.com
Greeting from Holypharm Biotech which is continuously building GMP quality system in China and good registration system.
It has been acceptable by US FDA through on-site inspection and dozens of DMFs were filed with US agency;
Besides, the GMP certificate was issued by European authority.
We can support you following APIs on both good ingredients and registration.
Pemetrexed disodium intermediate with DMF
Best regards
Jeffery Choo
Hangzhou Holypharm Biotech Co., Ltd.
Room 805, Building #2 British Center, European and American Financial City,Yuhang District, Hangzhou, China 310012
Mobile: +86 15824114678 Fax: +86-571-87357695
Email ID:jeffery@holypharm.com
Web: www.holypharm.com
