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1. Periactin (4 mg) Tablets - Nichi - Iko Pharmaceutical Brand. The required quantity is 6 boxes.
2. Penicillamine (250 mg) Tablets - Mylan Brand. The required quantity is 2 boxes.
3. Betahistine Dihydrochloride (8 mg) Tablets - Mylan Brand. The required quantity is 102 units.
4. Scopolamine Butyl bromide (20 mg/ ml) Injections - Sanofi/ Aventis Brand. The required quantity is 5 units.
5. Allopurinol (250 mg) Sustained-release Capsules - G.L. Pharma Gmbh Brand. The required quantity is 2 boxes.
Comments :
enquiry@healthbiotech.in
Hello There,
Greetings from Health Biotech Limited!
We are one of the leading Indian Pharmaceutical Manufacturer & Exporter of finished formulations. Our state-of-the-art, WHO-GMP certified manufacturing
facilities are located in the industrial town of Baddi, in the State of Himachal Pradesh, India.
We are a global exporter and kindly contact us +91 987-688-2973 or send email enquiry@healthbiotech.in
Thanks,
Jay
Health Biotech Limited
www.healthbiotech.in
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
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
