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1. Ceftriaxone Sodium (1 g & 2 g) Injections. The required quantity is 25,000 units & 23,000 units respectively.
2. Dexamethasone (4 mg ) Injections. The required quantity is 20,000 units.
3. Sodium Chloride (0.9% in 500 ml) Infusions. The required quantity is 18,500 units.
4. Methylprednisolone (40 mg) Ampoules. The required quantity is 15,000 units.
pradeepmarketing1999@gmail.com
pradeepmarketing1999@gmail.com share me this mail id , please
sidpatel6389@gmail.com
SIDDHA PHARMACY is presently one of India’s leading stockiest, Branded Pharmaceutical Exporter and Pharma Merchant Exporter for Private Label Pharma Manufacturing. Being a Branded Pharma Exporter we provide 100% original and are manufactured by well-known pharmaceutical manufacturers like Pfizer Inc, Novartis, GlaxoSmithKline Plc, Sanofi, Bayer AG, Eli Lilly and Co, Roche... 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.
SIDDHA PHARMACY
SIDPATEL6389@GMAIL.COM
WWW.SIDDHAPHARMA.COM
WWW.SIDDHAGLOBAL.COM
GSTIN – 24ACWFS1209B1ZB
IEC CODE – ACWFS1209B
CONTACT NO. / WHATSAPP NO. - +91-8866 86 2020
hostrinlifesciences@gmail.com
Dear friend,
Greetings from Hostrin Life Sciences!!!
We have been supporting the following services.
1.We do support DMF's for API's, Tech transfer support and 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's & Formulation's in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.
2. Impurity's & 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 and contract manufacturing services
6. Synthetic Resins technologies support.
7. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.
8. 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
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
