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FLUOXETINE

Active substance: fluoxetine

CAPSULE · FLUOXETINE HYDROCHLORIDE 20 mg/1

United StatesActive

Marketing holder: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

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
RU 25
  • Прозак®
    капсулы, 20 мг (original in Russian, GRLS)
    П N014206/01
    Общество с ограниченной ответственностью "Свикс Хэлскеа" (ООО "Свикс Хэлскеа")
  • Профлузак®
    капсулы, 20 мг (original in Russian, GRLS)
    ЛП-№(006534)-(РГ-RU)
    Акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (АО "АКРИХИН")
  • Профлузак®
    капсулы, 20 мг (original in Russian, GRLS)
    Р N003957/01
    Акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (АО "АКРИХИН")
  • Флуоксетин
    капсулы, 10 мг (original in Russian, GRLS)
    ЛП-№(001133)-(РГ-RU)
    Акционерное общество "Биоком" (АО "Биоком")
  • Флуоксетин
    капсулы, 20 мг (original in Russian, GRLS)
    ЛП-№(011894)-(РГ-RU)
    Общество с ограниченной ответственностью "Производство Медикаментов" (ООО "ПроМед")
All products in this country (25)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-3cd0-70d4-8873-8d41f9ba2975,01a120c3-7c23-7ccb-8e3c-2a9cbfeeea62,01a120c3-923d-70cf-9c38-21aa4867e54f,01a120c3-c7eb-79d1-85f7-93da9234b7d9,01a120c3-c93f-7ce7-b129-4ff15742609d;count=18 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-44a7-7c9a-87a4-d201bae69e83,01a1208c-4da4-752c-bc66-beecddeab41b,01a1208c-6243-7398-8294-efa2357078d9,01a1208c-6554-725d-94c5-5de18413472e,01a1208c-65a2-71ba-af48-243be18d294d;count=226 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
23155-029
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 23155-029 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 23155-029 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 23155-029 · Verified 2026-10-09 · open in source