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Cangrelor

Active substance: cangrelor

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · CANGRELOR 50 mg/1

United StatesActive

Marketing holder: Gland Pharma Limited

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
  • Kengrexal
    cangrelor
    EMEA/H/C/003773
    Chiesi Farmaceutici S.p.A.
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12090-9550-7bd5-963f-d1ec5ffded37,01a12093-3d74-7aae-8e52-619f1c6c5b1b;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
68083-412
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 68083-412 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 68083-412 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 68083-412 · Verified 2026-10-09 · open in source