06 Jul 2022

Reply

USP Grade Mupirocin (500 kg) API needed in India [ENA14244]
A company that deals in distribution of various pharmaceutical products is looking for suppliers of USP Grade Mupirocin (500 kg) API for commercial purpose. The suppliers must support this enquiry with CoA.

Comments :

shplexim@sohanhealthcare.com

Hi,
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. SHPL exports products to more than 30 countries and has more than 100 satisfied customers.
Our product details as per below
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 bipheny1)-4y1-1 H-Tetrazole.

Best & Regards,
Ramnath Pachpind
Mo +91-8552057638
shplexim@sohanhealthcare.com

17:40,  06 Jul 2022

chowdary@carbontree.in

We do supply Mupirocin API 500Kg

18:36,  06 Jul 2022

info@aeqpharma.com

hi,
We are biotech company.we sell Mupirocin API micronized and non, with support docs,EDQM,GMP,COA,DMF,CEP/COS...

21:06,  06 Jul 2022

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

13:38,  07 Jul 2022

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

13:39,  07 Jul 2022

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

00:58,  10 Jul 2022
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