Reply
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the APIs.
bdevomaar@gmail.com
crystalchemicalsfzllc@gmail.com
We can supply the following API, Please contact
Crystal Chemicals FZ-LLC
(Pharmaceuticals API's Distributor in UAE)
FDRK-3517, PO Box # 10055, Ras-AL-Khaimah, United Arab Emirates
(Whatsapp) +92-333-8484130
crystalchemicalsfzllc@gmail.com
www.crystalchemicals.com.pk
sales1@jnchsd.com
Dear Sir/Madam:
Greetings of the day. We are The Manuafacturer’s of API and Intermediates.
We, Shandong Chenghui Shuangda Pharmaceutical Co.,Ltd, are cGMP plant who manufactures the APIs and intermediates.
Some of our major products are mentioned below:
Vonoprazan Fumarate
LeterMovir
Dapagliflozin
Crisaborole
Sugammadex
Ropivacaine HCI
Tetracaine HCI
Tetracaine
Prilocaine
Lidocaine
Ozagrel Sodium
Celecoxib
Pramoxine HCI
Meldonium
We could supply above APIs and their main intermediates.
If you are intrested in any of them,please feel free to contact me by sales1@jnchsd.com
Tel:86-531-58897062,
Whatsapp/Wechat/Skype: +86 18605387751
Fiona
gauravkumar4368@gmail.com
Dear Sir / Madam,
We can offer various APIs. Kindly let us know your email id so that we can send you the email and we can give you the best price.
Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA
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
Whatsapp +91 9033215377
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE
chowdary@carbontree.in
Dear Sir,
We can supply Sacubitril +Valsartan from our EUGMP certified facility with DMF. Please let us know your quantity requirement.
Regards
PA Chowdary
chowdary@carbontree.in
chowdary@carbontree.in
Dear Sir,
We can supply Sacubitril +Valsartan from our EUGMP certified facility with DMF. Please let us know your quantity requirement.
We have ready stocks 50-100Kg lots
Regards
PA Chowdary
chowdary@carbontree.in
Krishna@hrvglobal.com
Please mail me
info@attichem.com
We can supply the following API, Please contact
us immediately with your inquiry in order to communicate with you directly.
I hope to hear from you.
Regards,
Miss Laurel Williams
Attic Chemical, Inc, USA
sales1@jnchsd.com
Dear Sir/Madam:
Greetings of the day. We are The Manuafacturer’s of API and Intermediates.
We, Shandong Chenghui Shuangda Pharmaceutical Co.,Ltd, are cGMP plant who manufactures the APIs and intermediates.
Some of our major products are mentioned below:
Vonoprazan Fumarate
LeterMovir
Dapagliflozin
Crisaborole
Sugammadex
Ropivacaine HCI
Tetracaine HCI
Tetracaine
Prilocaine
Lidocaine
Ozagrel Sodium
Celecoxib
Pramoxine HCI
Meldonium
We could supply above APIs and their main intermediates.
If you are intrested in any of them,please feel free to contact me by sales1@jnchsd.com
Tel:86-531-58897062,
Whatsapp/Wechat/Skype: +86 18605387751
Fiona
harshavardhan.b@hetero.com
Hi,good morning
From Hetero.
Please send enquiry to below mail
harshavardhan.b@hetero.com
Hi,good morning
From Hetero.
Please send enquiry to below mail
ravisankar.cherukuru@amaralabs.in
Dear Sir,
We can supply Sacubitril +Valsartan from our EUGMP certified facility with DMF. Please let us know your quantity requirement.
Ref web site: www.amaralabs.in
Regards
Ravi sankar
sales@clearsynthlab.com
Reply:
1- Sacubitril API
2- Valsartan API
Clearsynth demonstrates the ability to consistently provide products and services that meet customer and regulatory requirements. Kindly confirm your requirement by email so we can provide the Quotation, COA within 24hrs Max from the inquiry date.
Regards
Mr. V. Ambati
International Sales & Business Development
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
+91-9394436878
sales@clearsynthlab.com
smit@salvavidaspharma.com
Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers and it can be available with us.
can we connect for some business?
Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )
hostrinlifesciences@gmail.com
Dear friend,
Greetings from Hostrin Life Sciences!!!
We have been supporting the following services.
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA. DMF's for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/FDA with 5 modules including BA and BE studies /Clinical studies/trials for finished formulation's in Pharmaceutical, ayurveda, Biotech, Biosimilar, vitamins , Peptides and Transdermal patches too.
2. eCTD publishing with potential software, addressing post submission queries from all regulatory authorities and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.
3. Impurity's & Reference standards support for API's
4. Services for IPR & Regulatory compliance
5. Services for QMS & supporting of QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars companies who are willing to enter into the Regulatory market which is mandatory to show for FDA.
6. Custom synthesis and contract manufacturing services
7. Synthetic Resins technologies support.
8. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.
9. Pharmacovigilance services.
Pls don't hesitate to send your inquiries. For your reference, please go through our website www.hostringlobal.com
For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
hostrinlifesciences@gmail.com
Dear friend,
Greetings from Hostrin Life Sciences!!!
We have been supporting the following services.
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA. DMF's for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/FDA with 5 modules including BA and BE studies /Clinical studies/trials for finished formulation's in Pharmaceutical, ayurveda, Biotech, Biosimilar, vitamins , Peptides and Transdermal patches too.
2. eCTD publishing with potential software, addressing post submission queries from all regulatory authorities and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.
3. Impurity's & Reference standards support for API's
4. Services for IPR & Regulatory compliance
5. Services for QMS & supporting of QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars companies who are willing to enter into the Regulatory market which is mandatory to show for FDA.
6. Custom synthesis and contract manufacturing services
7. Synthetic Resins technologies support.
8. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.
9. Pharmacovigilance services.
Pls don't hesitate to send your inquiries. For your reference, please go through our website www.hostringlobal.com
For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
shplexim@sohanhealthcare.com
Sohan Healthcare Pvt Ltd is engaged in manufacturing of Active Pharmaceuticals Ingredients, Semi Finished formulations. The facility is audited and approved by European Authority, Russian Authority, Korea MFDS. Our facility is also USFDA complied. We hold CEP for Metformin HCl API
Metformin HCL EP/BP/IP/USP/CEP
Metformin DC Granules 86.66% / 93.60% / 95% / 90% / 83.33%.
Gliclazide EP/BP/IP/CEP
Folic Acid- IP, USP
(TTBB) 3- tripheny1-methy1-5(4-bromo methy1)(1,1 bipheny
