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SANCUSO

Active substance: granisetron

PATCH · GRANISETRON 3.1 mg/24h

United StatesActive

Marketing holder: Cumberland 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
  • Sancuso
    granisetron
    EMEA/H/C/002296
    Grünenthal GmbH
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-8f5f-7bc9-8d89-9b61f515d2bc,01a1208c-af40-7ef4-a55f-9099fe3d6323,01a1208d-3b02-76f9-bf35-d87cee8885ef,01a1208d-70ec-7d51-95d9-e0b6b8790b11,01a1208d-7bce-7ddc-960a-2a0b3b685157;count=14 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
66220-637
Registration status
Active
Dispensing
Prescription only
Route
TRANSDERMAL
Sources
  • product · openFDA NDC · 66220-637 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 66220-637 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 66220-637 · Verified 2026-10-09 · open in source