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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
info@eqpharma.com
we supply Chlorpheniramine Maleate API
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
sales@bozera.com
we can offer you Chlorpheniramine Maleate with good price. pls kindly send us mail for more discussion. sale@bozera.com
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
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
sales@clearsynthlab.com
Re: EP/ USP Grade Chlorpheniramine Maleate (2 MT) 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
clearsynthlab.com
sales@clearsynthlab.com
