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Amifostine Trihydrate

Active substance: amifostine

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · AMIFOSTINE 500 mg/1

United StatesActive

Marketing holder: Symbiosis Pharmaceutical Services Limited

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208d-ff7e-7398-9a3e-7916c18fcd8b,01a12092-fbd8-7115-8ab1-e567daad460b;count=2 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
84684-001
Registration status
Active
Dispensing
Prescription only
Sources
  • product · openFDA NDC · 84684-001 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 84684-001 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 84684-001 · Verified 2026-10-09 · open in source