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Attruby

Active substance: acoramidis

TABLET, FILM COATED · ACORAMIDIS HYDROCHLORIDE 356 mg/1

United StatesActive

Marketing holder: BridgeBio Pharma, 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
  • Beyonttra
    acoramidis hydrochloride
    EMEA/H/C/006333
    Bayer AG 
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12091-13c2-7a36-8ec3-65f954ccfdf8;count=1 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
82228-712
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 82228-712 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 82228-712 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 82228-712 · Verified 2026-10-09 · open in source