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Dexrazoxane

Active substance: dexrazoxane

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · DEXRAZOXANE HYDROCHLORIDE 250 mg/1

United StatesActive

Marketing holder: Hikma Pharmaceuticals USA 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
  • Savene
    dexrazoxane hydrochloride
    EMEA/H/C/000682
    CNX Therapeutics Ireland Limited
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2afd-721d-b284-5e3223187d74,01a1208c-2afd-7e41-b284-5e3223fcbc24,01a1208c-2b14-7ee4-8dd0-21bf69a74cac,01a1208c-a4fa-7f7d-ba97-d21415ad0b00,01a1208d-bbb5-75b6-908c-adda0da3a0d8;count=11 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0143-9247
Registration status
Active
Dispensing
Prescription only
Route
INTRAVENOUS
Sources
  • product · openFDA NDC · 0143-9247 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0143-9247 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0143-9247 · Verified 2026-10-09 · open in source