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Pralatrexate

Active substance: pralatrexate

INJECTION · PRALATREXATE 40 mg/2mL

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 1
  • Folotyn
    pralatrexate
    EMEA/H/C/002096
    Allos Therapeutics Ltd
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208d-be1c-7d86-bef7-d630432f1770,01a1208e-af88-7593-9907-40568c8715d7,01a1208f-afe2-780d-9649-a5523a76848a,01a1208f-afe5-7cf5-a5b2-55526984f64d,01a12099-1a5d-7f40-b653-0817aed1a564;count=6 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
43598-343
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 43598-343 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 43598-343 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 43598-343 · Verified 2026-10-09 · open in source