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Zartra

Active substance: imiquimod

imiquimod

Centralised EU authorisationWithdrawn

Marketing holder: Laboratoires 3M Santé

Verified 2026-10-09 · EMA

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
US 14
  • IMIQUIMOD
    CREAM · IMIQUIMOD 12.5 mg/.25g
    72189-084
    DIRECT RX
  • Imiquimod
    CREAM · IMIQUIMOD 50 mg/g
    51672-4145
    Sun Pharmaceutical Industries, Inc.
  • Imiquimod
    CREAM · IMIQUIMOD 37.5 mg/g
    0093-3133
    Teva Pharmaceuticals USA, Inc.
  • Imiquimod
    CREAM · IMIQUIMOD 37.5 mg/g
    87519-004
    Anvi Pharmaceuticals Inc.
  • Imiquimod
    CREAM · IMIQUIMOD 12.5 mg/.25g
    71335-2725
    Bryant Ranch Prepack
All products in this country (14)
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-71de-77dd-8a50-27e3b5dd2f98,01a1208c-fdd3-77f7-843b-c85d41ebb8b2,01a1208d-f492-7b16-96f9-d99fde0dd9ba,01a1208e-f23c-7f93-9e5b-4fdcf1551d1e,01a12091-6764-7d0a-8c0a-d4deb4f3a5ad;count=14 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/000180
Registration status
Withdrawn
ATC code
L03AX
Sources
  • product · EMA · EMEA/H/C/000180 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/000180 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/000180 · Verified 2026-10-09