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Olanzapine Viatris (previously Olanzapine Mylan)

Active substance: olanzapine

olanzapine

Centralised EU authorisationActive

Marketing holder: Viatris Limited

Verified 2026-10-09 · EMA

Analogues in other countries
Composition
Analogues by country

Products with the same active substance registered in other countries.

CountryProducts
RU 46
  • Заласта®
    таблетки, 10 мг (original in Russian, GRLS)
    ЛП-№(001778)-(РГ-RU)
    АО "КРКА, д.д., Ново место"
  • Заласта®
    таблетки, 10 мг (original in Russian, GRLS)
    ЛСР-005811/09
    АО "КРКА, д.д., Ново место"
  • Заласта® Ку-таб®
    таблетки, диспергируемые в полости рта, 10 мг (original in Russian, GRLS)
    ЛП-№(001780)-(РГ-RU)
    АО "КРКА, д.д., Ново место"
  • Заласта® Ку-таб®
    таблетки, диспергируемые в полости рта, 10 мг (original in Russian, GRLS)
    ЛСР-005803/09
    АО "КРКА, д.д., Ново место"
  • Зипрекса®
    таблетки, покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    ЛП-№(011108)-(РГ-RU)
    Чеплафарм Реджистрейшн ГмбХ
All products in this country (46)
US 238
  • LYBALVI
    TABLET, FILM COATED · OLANZAPINE 5 mg/1, SAMIDORPHAN L-MALATE 10 mg/1
    65757-651
    Alkermes, Inc.
  • LYBALVI
    TABLET, FILM COATED · OLANZAPINE 10 mg/1, SAMIDORPHAN L-MALATE 10 mg/1
    65757-652
    Alkermes, Inc.
  • LYBALVI
    TABLET, FILM COATED · OLANZAPINE 15 mg/1, SAMIDORPHAN L-MALATE 10 mg/1
    65757-653
    Alkermes, Inc.
  • LYBALVI
    TABLET, FILM COATED · OLANZAPINE 20 mg/1, SAMIDORPHAN L-MALATE 10 mg/1
    65757-654
    Alkermes, Inc.
  • OLANZAPINE
    TABLET · OLANZAPINE 20 mg/1
    72303-0840
    HEC Pharm USA Inc.
All products in this country (238)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-317c-7731-9785-9cf5dddf6413,01a120c3-3781-7c84-bd79-807a28ef1276,01a120c3-4316-7bd4-85ea-08cc25527c0c,01a120c3-4319-7d8f-975d-bb4804804773,01a120c3-47ec-746c-a650-3486248b6a76;count=38 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2b09-70fe-8721-523de21808f5,01a1208c-2b41-740b-af96-847a006b93be,01a1208c-2b42-700d-b302-27cdd1218e05,01a1208c-2ca8-7a00-8eb1-823de4c9c554,01a1208c-2ca9-7690-80bc-fa44b43546f6;count=219 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/000961
Registration status
Active
ATC code
N05AH03
Sources
  • product · EMA · EMEA/H/C/000961 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/000961 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/000961 · Verified 2026-10-09