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FLUDARA FOR INTRAVENOUS INJECTION 50mg/VIAL

Product Information

Registration Status: Active

SIN11143P

FLUDARA FOR INTRAVENOUS INJECTION 50mg/VIAL is approved to be sold in Singapore with effective from 1999-05-10. It is marketed by SANOFI-AVENTIS SINGAPORE PTE LTD, with the registration number of SIN11143P.

This product contains Fludarabine Phosphate 50mg/vial in the form of INJECTION, POWDER, FOR SOLUTION. It is approved for INTRAVENOUS use.

This product is manufactured by INTENDIS MANUFACTURING SPA in ITALY, andBAXTER ONCOLOGY GmbH 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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