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STRENSIQ

Active substance: asfotase alfa

SOLUTION · ASFOTASE ALFA 28 mg/.7mL

United StatesActive

Marketing holder: Alexion Pharmaceuticals, 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
  • Strensiq
    asfotase alfa
    EMEA/H/C/003794
    Alexion Europe SAS
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-4dd3-7b4c-bffe-79ee208f8f9f,01a1208c-4dd5-71a2-9db3-c7c25bf06217,01a1208d-040b-7048-ab85-abc5185d5ef1,01a1209d-0b6d-7896-be79-7af572b58bee;count=4 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
25682-013
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 25682-013 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 25682-013 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 25682-013 · Verified 2026-10-09 · open in source