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DEFERIPRONE

Active substance: deferiprone

TABLET, COATED · DEFERIPRONE 500 mg/1

United StatesActive

Marketing holder: DR. REDDY'S LABORATORIES, 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 3
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-461c-7a03-92e1-360f3cdfb893,01a1208d-be71-7f0b-b83a-8f1aa5b6c5c8,01a1208e-ceee-7db3-8b99-ed34b1525fb1,01a12091-6921-7f1e-8573-ad21760b46b7,01a12092-7849-7559-a3a1-a15c7c389ed7;count=10 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
75907-349
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 75907-349 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 75907-349 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 75907-349 · Verified 2026-10-09 · open in source