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1. Famotidine (20 mg) Powder and solvent for solution for Injections. The required quantity is 110,000 units.
2. Silymarin (90 mg) Capsules. The required quantity is 55,000 units.
3. Ascorbic Acid (100 mg/ ml in 5 ml) Solution for Injections. The required quantity is 180,000 units.
4. Dexamethasone (4 mg/ ml in 1 ml) Solution for Injections. The required quantity is 80,000 units.
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pharmahouse@ymail.com
Services offered by PHARMA HOUSE
Dossiers (CTD, e-CTD, ANDA and ANVISA)
(All Country Specific, As per client request)
DMFs(CTD, e-CTD)(Open &Closed part)
(All Regions and Country regulations)
Technology transfers(API'S &Formulations),
( Paper technology & Product Development)
Pharmacovigilance(PV),
Intellectual properties(IP)
We have seperate Teams for Product Development for API'S &Formulations.
All product Documentations (Process, training, trouble shooting)
&other Regulatory services
Pharma House,
What's App & Voice:+91 81433 69525
pharmahouse@ymail.com ,
Hyderabad, India
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
harshad976@gmail.com
"Greetings for the day !
I take this opportunity to write to you with introduction of our Pharmaceuticals company same established in year 2007 and we have valid approval like US-FDA, UK-MHRA, Anvisa, TGA, WHO-GMP Etc.
We offer API, Intermediates and FDF products from Regulatory approved plant.
"
info@aidotickpharma.com
Aidotick Pharmaceutical is a leading pharmaceutical company based in India with an excellent reputation on the market. With years of experience in developing, contract manufacturing and exporting a broad range of pharmaceutical products, Aidotick has established a strong foothold across Latin America, Africa, South East Asia, the Middle East, and many other locations around the world.
If you looking for a pharmaceutical manufacturer or supplier that assures premium quality with outstanding packaging at extremely affordable prices, we can discuss further and can provide you our company profile, product list and quotes.
Please contact us on the given details so that we can communicate further.
Call / WhatsApp: +91 99790 56769 ( https://wa.me/919979056769 )
Email: marketing@aidotickpharmaceuticals.com, info@aidotickpharma.com
Website: https://aidotickpharma.com/
Waiting for the long term collaboration and positive reply from your end.
Thank you.
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.
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
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
pooja.arane@zenvisionpharma.com
I am Pooja Arane from Zenvision pharma.
Contact Details:
Mob -9137027167
Email-pooja.arane@zenvisionpharma.com
Zenvision Pharma LLP is a contract research & development organization based in Navi Mumbai, India; offering full range of custom designed formulation development services with professional standards. We offer turnkey product development services for Generic and Specialty pharmaceuticals.
