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PLERIXAFOR

Active substance: plerixafor

INJECTION · PLERIXAFOR 24 mg/1.2mL

United StatesActive

Marketing holder: Zydus Lifesciences Limited

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 2
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-29a9-7062-bef6-211017b58cca,01a1208c-7723-73ca-8c89-719c9f079c06,01a1208c-989d-7d70-88ab-3f15084fc3d8,01a1208d-03d8-7095-af8d-cf4fa96ad05d,01a1208d-05c2-7eb3-aa18-3e323719248c;count=13 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
70771-1776
Registration status
Active
Dispensing
Prescription only
Route
SUBCUTANEOUS
Sources
  • product · openFDA NDC · 70771-1776 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 70771-1776 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 70771-1776 · Verified 2026-10-09 · open in source