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1. Lisdexamfetamine Dimesylate (10 mg) Capsules. The required quantity is 383 packs for first year, 947 packs for second year, 1,381 packs for third year & 1,590 packs for fourth year.
2. Lisdexamfetamine Dimesylate (20 mg) Capsules. The required quantity is 383 packs for first year, 947 packs for second year, 1,381 packs for third year & 1,590 packs for fourth year.
3. Lisdexamfetamine Dimesylate (30 mg) Capsules. The required quantity is 1,915 packs for first year, 4,733 packs for second year, 6,906 packs for third year & 7,950 packs for fourth year.
4. Lisdexamfetamine Dimesylate (40 mg) Capsules. The required quantity is 2,808 packs for first year, 6,941 packs for second year, 10,128 packs for third year & 11,660 packs for fourth year.
5. Lisdexamfetamine Dimesylate (50 mg & 60 mg) Capsules. The required quantity is 2,553 packs for first year, 6,310 packs for second year, 9,208 packs for third year & 10,600 packs for fourth year respectively.
6. Lisdexamfetamine Dimesylate (70 mg) Capsules. The required quantity is 1,276 packs for first year, 3,155 packs for second year, 4,604 packs for third year & 5,300 packs for fourth year.
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info@indeximinternational.com
INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, 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
info@indeximinternational.com
INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, 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
hostrinlifesciences@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
marketing@endofar.com
Dear Friend
We believe that we can fulfill your requirements.
Please contact us on following details.
E-mail: Marketing@Endofar.com
I’m waiting for your kind email.
ENDOFAR Ilac Co. is a pharmaceutical company in Istanbul, Turkey. Our portfolio contains several specific #APIs & #Finished Dosage form medications in the field of Natural #Cannabinoid & #Opioid medications, #Cosmeceuticals & also #Nutraceutical Supplements.
SPECIAL OFFER from ENDOFAR ?laç
1. API Supply
2. Manufacturing Products with Your Own Label
3. Technical & Scientific Supports
4. Flexible Payment Terms
5. Providing CTD/ FORMULLA for FDFs
6. European Out-Licensing
