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ADYNOVATE 500 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION

Product Information

Registration Status: Active

ADYNOVATE 500 IU POWDER AND SOLVENT FOR SOLUTION FOR INJECTION is approved to be sold in Singapore with effective from 2020-11-24. It is marketed by TAKEDA PHARMACEUTICALS (ASIA PACIFIC) PTE LTD, with the registration number of SIN16049P.

This product contains Rurioctocog Alfa Pegol 500IU in the form of INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION. It is approved for INTRAVENOUS use.

This product is manufactured by Baxalta Manufacturing Sarl (bulk production and primary packager) in SWITZERLAND, andSiegfried Hameln GmbH (Diluent) in GERMANY.

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.

References

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

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