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Optruma

Active substance: raloxifene

raloxifene hydrochloride

Centralised EU authorisationActive

Marketing holder: Eli Lilly Nederland B.V.

Verified 2026-10-09 · EMA

Analogues in other countries
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
US 23All products in this country (23)
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2737-7e95-9c31-45c2b75ab1f1,01a1208c-4aad-7704-882f-655eb5dedacf,01a1208c-682f-736f-b9fe-b1ee0bf60ee0,01a1208c-f23c-77c5-afb4-75c84465e31f,01a1208d-7025-7160-9739-b5e5d32d4e26;count=23 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/000185
Registration status
Active
ATC code
G03XC01
Sources
  • product · EMA · EMEA/H/C/000185 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/000185 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/000185 · Verified 2026-10-09