24 Jan 2022

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Various Finished Dosage Formulations needed in Brazil [ENA12490]
A company that deals in the research, development & trading of health products is looking for suppliers of Various Finished Dosage Formulations for commercial purpose. The suppliers must support this enquiry with CTD Dossier, ANVISA, DMF & PIC/s GMP.
1. Zolpidem Tartrate (5 mg) SR Tablets. The required quantity is 50 million units.
2. Ondansetron (4 mg & 8 mg) Tablets. The required quantity is 15 million units for each.
3. Azithromycin (500 mg) Film-coated Tablets. The required quantity is 18.5 million units.
4. Azithromycin (22.5 ml & 37.5 ml) Suspensions. The required quantity is 3 million units & 2 million units respectively.
5. Azithromycin (500 mg) Lyophilized Vials. The required quantity is 10 million units.
6. Daratumumab (1800 mg in 15 ml, 400 mg in 20 ml & 100 mg in 5 ml) Ampoules. The required quantity is 50 million units, 50 million units & 20 million units respectively.

Comments :

info@indeximinternational.com

Kindly mail your requirements
INDEXIM INTERNATIONAL, one of the leading manuafcturer, suppliers, exporter and importer of 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
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

12:12,  24 Jan 2022

sidpatel6389@gmail.com

SIDDHA PHARMACY is presently Pharmaceutical Exporter and Pharma Merchant Exporter for Private Label Pharma Manufacturing. Being a Pharma Exporter we provide customized solution for our customers. We have our biggest market in EMEA as Branded Pharma Exporter and Branded Medicine Exporter owing to our quality service and best prices provided to our customer. We also work with clusters of manufacturers for White Label Manufacturing having the following certification: WHO GMP, EU-GMP, PIC/s, UKMHRA etc.

We can provide you above requirements with needed documents supports.
Awaiting for your valuable response for the same.

Thanks & Regards,
Siddharth Patel
Siddha Pharmacy
+91-8866 86 2020
WWW.SIDDHAGLOBAL.COM
WWW.SIDDHAPHARMA.COM
GSTIN – 24ACWFS1209B1ZB
IEC CODE – ACWFS1209B

12:36,  24 Jan 2022

jgq@yangzijiang.com

I am Justin from Yangtze River Pharmaceutical Group in China

APIs and generic Drugs (FDF) can be supplied 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

07:06,  25 Jan 2022

himali.pawaskar@dksh.com

Hi, Please share this lead .

12:08,  25 Jan 2022

yangxiaoqing2@ncpc.biz

NCPC is one of the largest pharmaceutical enterprises in China covering more than 600 kinds of APIs and preparations such as antibiotics,semisynthetic antibiotics, vitamins, biological, Veterinary drugs, etc.
We have passed GMP audit from many authorities including FDA, EDQM, ANVISA,MHRA, PMDA, WHO, INVIMA, etc. And we are qualified supplier of GSK, Sanofi-Aventis, UNICEF, MSF and PFSCM.
Please contact us for further information.
We're sure your any inquiry will get prompt attention.

11:16,  26 Jan 2022

hostrinlifesciences@gmail.com

Dear Friends,

Greetings from Hostrin Life sciences!!!

Greetings from CRISTONE LIFE CARE !!!

We have been supporting the following services.

1.We do support DMF for API, Tech transfer support,Compilation/Registration of Dossiers in MOH /MHRA/EMEA/USA support in CTD, ACTD, eCTD and ANDA's formats with 5 modules including BA and BE studies /Clinical studies/trials for API & Formulations in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.
2. Impurities & Reference standards support for API's
3. Services for IPR & Regulatory compliance
4. 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.
5. Custom synthesis & Contract manufacturing services
6. Synthetic Resins technologies support
Pls don't hesitate to send your inquiry. For your reference please go through our website www.hostringlobal.com.

7. We have been exporting various finished formulations, API's, Biotech & Biosimilar products from CRISTONE LIFE CARE, please visit our website: www.cristoneglobal.com for supply.
Please send your enquiries to cristonelifecare@gmail.com.

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com/andrew@hostringlobal.com
Mobile/WhatsApp: +91 9949930343

19:32,  27 Jan 2022

sumit@saappharma.com

Dear Sir,

We have EU approved Source for several products listed in the Message.
Pl contact - sumit@saappharma.com

16:20,  22 Feb 2022

sumit@saappharma.com

Dear Sir,

We have EU approved Source for several products listed in the Message.
Pl contact - sumit@saappharma.com

16:20,  22 Feb 2022
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