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MEMANTINE AND DONEPEZIL HYDROCHLORIDES

Active substance: MEMANTINE HYDROCHLORIDE, DONEPEZIL HYDROCHLORIDE

CAPSULE, EXTENDED RELEASE · MEMANTINE HYDROCHLORIDE 21 mg/1, DONEPEZIL HYDROCHLORIDE 10 mg/1

United StatesActive

Marketing holder: ANI Pharmaceuticals, Inc.

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
Products containing memantine in other countries

Showing products with this active substance, combinations included; the full composition is shown for each product.

CountryProducts
RU 84
  • Акатинол Мемантин
    таблетки, покрытые пленочной оболочкой, 20 мг (original in Russian, GRLS)
    ЛП-№(014661)-(РГ-RU)
    Мерц Фарма ГмбХ и Ко. КГаА
  • Акатинол Мемантин
    таблетки, покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    ЛП-№(014747)-(РГ-RU)
    Мерц Фарма ГмбХ и Ко. КГаА
  • Акатинол Мемантин
    таблетки, покрытые пленочной оболочкой, 20 мг (original in Russian, GRLS)
    ЛП-000652
    Мерц Фарма ГмбХ и Ко. КГаА
  • Акатинол Мемантин
    набор таблеток, покрытых пленочной оболочкой, 5 мг+10 мг+15 мг+20 мг [набор] (original in Russian, GRLS)
    ЛП-001433
    Мерц Фарма ГмбХ и Ко. КГаА
  • Акатинол Мемантин
    таблетки, покрытые пленочной оболочкой, 10 мг (original in Russian, GRLS)
    П N014961/01
    Мерц Фарма ГмбХ и Ко. КГаА
All products in this country (84)
EU 12
  • Acrescent
    memantine hydrochloride, donepezil hydrochloride
    EMEA/H/C/002424
    H. Lundbeck A/S
  • Axura
    memantine hydrochloride
    EMEA/H/C/000378
    Merz Pharmaceuticals GmbH
  • Balaxur
    memantine hydrochloride, donepezil hydrochloride
    EMEA/H/C/002708
    Merz Pharmaceuticals GmbH
  • Ebixa
    memantine hydrochloride
    EMEA/H/C/000463
    H. Lundbeck A/S
  • Marixino (previously Maruxa)
    memantine hydrochloride
    EMEA/H/C/002658
    KRKA, d.d.
All products in this country (12)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-2e6e-70a5-9db7-551fc81b86d1,01a120c3-2f91-7464-8bb8-65b07d9b04f3,01a120c3-2faa-7957-ba9f-46172924c591,01a120c3-43bc-77ed-8b34-77c8c3553f98,01a120c3-45ad-7ca3-bc6c-2c13fec35706;count=67 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-36e7-7f31-95d0-4c83e327f0ec,01a1208c-3fef-76a7-a723-c88585780e8b,01a1208c-420d-7c24-bc20-932e4882e6e4,01a1208c-4212-7896-bd8d-45df87c93bd6,01a1208c-505c-7386-bf55-ec4f326564e9;count=123 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
62559-207
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 62559-207 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 62559-207 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 62559-207 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 62559-207 · Verified 2026-10-09 · open in source