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ELAPRASE

Active substance: idursulfase

SOLUTION, CONCENTRATE · IDURSULFASE 6 mg/3mL

United StatesActive

Marketing holder: Takeda Pharmaceuticals America, Inc.

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
EU 1
  • Elaprase
    idursulfase
    EMEA/H/C/000700
    Takeda Pharmaceuticals International AG Ireland Branch
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1209d-83cf-74e9-a312-7848ab10c053;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
54092-700
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 54092-700 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 54092-700 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 54092-700 · Verified 2026-10-09 · open in source