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DENGVAXIA, POWDER AND SOLVENT FOR SUSPENSION FOR INJECTION

Product Information

Registration Status: Active

SIN15096P

DENGVAXIA, POWDER AND SOLVENT FOR SUSPENSION FOR INJECTION is approved to be sold in Singapore with effective from 2016-10-11. It is marketed by SANOFI-AVENTIS SINGAPORE PTE LTD, with the registration number of SIN15096P.

This product contains CYD Dengue Virus Serotype 1 Each strain: 4.5 - 6.0 log10 CCID50/dose,CYD Dengue Virus Serotype 2 ,CYD Dengue Virus Serotype 3 , and CYD Dengue Virus Serotype 4 in the form of SUBCUTANEOUS INJECTION, POWDER, FOR SUSPENSION. It is approved for SUBCUTANEOUS use.

This product is manufactured by Sanofi Pasteur (VDR) in FRANCE.

It is a Prescription Only Medicine that can only be obtained from a doctor or a dentist, or a pharmacist with a prescription from a Singapore-registered doctor or dentist.

Product Reference
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Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.



Source of information: Drugbank (External Link). Last updated on: 3rd July 18. *Trade Name used in the content below may not be the same as the HSA-registered product.

References

  1. Health Science Authority of Singapore - Reclassified POM
  2. Drugbank

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