Product Information

Registration Status: Active

FEIBA NF 500 U is approved to be sold in Singapore with effective from 1999-04-20. It is marketed by SHIRE SINGAPORE PTE LTD, with the registration number of SIN10889P.

This product contains Coagulation Factor IX/II/VII/X (Combination) 25 u/ml in the form of INJECTION, POWDER, FOR SOLUTION. It is approved for INTRAVENOUS use.

This product is manufactured by BAXTER AG in AUSTRIA, andSiegfried Hameln GmbH (Solvent) 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.

Coagulation Factor IX/II/VII/X (Combination)

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.


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