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sevelamer hydrochloride

Active substance: sevelamer

TABLET, FILM COATED · SEVELAMER HYDROCHLORIDE 800 mg/1

United StatesActive

Marketing holder: Cardinal Health 107, LLC

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 2
  • Renagel
    sevelamer
    EMEA/H/C/000254
    Sanofi Winthrop Industrie
  • Tasermity
    sevelamer hydrochloride
    EMEA/H/C/003968
    Genzyme Europe BV
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208e-1b1c-73d0-ba7a-f2b0a87fb79d,01a1208e-77ca-776d-b565-382bdc1c1544,01a1208f-004d-7974-b903-69268dea9489,01a12090-995b-7248-a640-bfaa78c09df5,01a12091-6771-77e3-ab3f-444cd83cc7ed;count=13 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
55154-2647
Registration status
Active
Dispensing
Prescription only
Route
PARENTERAL
Sources
  • product · openFDA NDC · 55154-2647 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 55154-2647 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 55154-2647 · Verified 2026-10-09 · open in source