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QUINIDINE SULFATE

Active substance: quinidine

TABLET · QUINIDINE SULFATE 200 mg/1

United StatesActive

Marketing holder: EPIC PHARMA, 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 1
  • Nuedexta
    dextromethorphan, quinidine
    EMEA/H/C/002560
    Jenson Pharmaceutical Services Limited
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a12093-6a6c-7d77-945a-2bcb862da09f,01a1209a-e67c-7167-87eb-71996819b86e;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
42806-513
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 42806-513 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 42806-513 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 42806-513 · Verified 2026-10-09 · open in source