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1. Clindamycin 100 mg + Clotrimazole 200 mg suppositories.
2. Clindamycin 100 mg + Clotrimazole 100 mg + Tinidazole 100 mg suppositories.
3. Metronidazole 500 mg + Neomycin sulfate 65 000 IU + Nystatin 100 000 IU suppositories.
4. Neomycin 83 mg + Metronidazole 500 mg + Clotrimazole 100 mg suppositories.
5. Metamizole 400 mg + Drotaverine hydrochloride 40 mg + Caffeine 60 mg Tablets.
6. Ibuprofen 400 mg + Drotaverine hydrochloride 80 mg Tablets.
7. Drotaverine 80 mg + Paracetamol 500 mg Tablets.
8. Drotaverine 80 mg + Mefenamic acid 250 mg Tablets.
9. Dicycloverine 10 mg + Mefenamic acid 250 mg Tablets.
10. Dicycloverine 20 mg + Paracetamol 500 mg + Mefenamic acid 250 mg Tablets.
11. Orphenadrine citrate 35 mg + Mefenamic acid 250 mg Tablets.
12. Orphenadrine citrate 50 mg + Aspirin 770 mg + Caffeine 60 mg Tablets.
13. Hyoscine butylbromide 10 mg + Ketoprofen 100 mg Tablets.
14. Hyoscine butylbromide 20 mg + Ibuprofen 400 mg + Caffeine 50 mg Tablets.
15. Hyoscine butylbromide 20 mg + Ibuprofen 400 mg Tablets.
16. Hyoscine butylbromide 10 mg + Metamizole 250 mg Tablets.
17. Hyoscine butylbromide 10 mg + Paracetamol 500 mg Tablets.
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Cristonelifecare@gmail.com
Dear Friend,
Greetings from Hostrin Life Sciences!!!
Hostrin offers the following services:
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.
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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.
3. Support for Impurity's, Reference standards and RLD's
4. Services for IPR & Regulatory compliance with all risk assessments.
5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.
6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.
7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.
8. Synthetic Resin technologies support.
9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.
10. Pharmacovigilance services.
Pls don't hesitate to send your inquiries. For your reference, please go through our website www.hostringlobal.com
For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
www.hostringlobal.com
aakashdomadia@gmail.com
Dear sir ,
Can help you with your requirements kindly send us an email and will provide u with best rates
