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1. Doxazosin (4 mg) Tablets. The required quantity is 5,400 units.
2. Norepinephrine (1 mg/ ml in 4 ml) Solution for Infusions. The required quantity is 6,000 units.
3. L-Ornithine L-aspartate (150 mg) Tablets. The required quantity is 9,200 units.
4. Budesonide (0.25 mg/ 2 ml) Ampoules. The required quantity is 6,000 units.
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 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
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 currently export to more than 51 countries. We frequently export
to regions like CIS, LATAM, Middle East, Africa, South Asia and many more.
Our Product Range :
Dry & Liquid Injectables, Pre-Filled Syringes, Betalactum Injectables, Tablets, Capsules, Soft Gelatin Capsules, Dry Syrups, Liquid Orals, Eye/Ear Drops,
Effervescent & Mouth Dissolving Tablets, Ointments, Dental Cartridges, Suppositories, IV Fluids
Our Product Category :
Anti Covid19, AntiRetroVirals, Antibiotics, Oncology, Cardiovascular, Hormones, Gastrointestinal
Our Services
PCD Pharma Franchise, CRAMS / Contract Manufacturing, Loan Licensing, Institutional sale etc.
Kindly contact us +91 987-688-2973 or send email enquiry@healthbiotech.in
Thanks,
Health Biotech Limited
Phone : +91 987 688 2973
Email : enquiry@healthbiotech.in
Website : www.healthbiotech.in
