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Nevirapine Teva

Active substance: nevirapine

nevirapine

Centralised EU authorisationWithdrawn

Marketing holder: Teva B.V. 

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 22
  • Вирамун®
    суспензия для приема внутрь, 50 мг/5 мл, 240 мл (original in Russian, GRLS)
    ЛП-№(006248)-(РГ-RU)
    Берингер Ингельхайм Интернешнл ГмбХ
  • Вирамун®
    суспензия для приема внутрь, 50 мг/5 мл, 240 мл (original in Russian, GRLS)
    П N011661/01
    Берингер Ингельхайм Интернешнл ГмбХ
  • Невирапин
    суспензия для приема внутрь, 10 мг/мл, 240 мл (original in Russian, GRLS)
    ЛП-№(012596)-(РГ-RU)
    Акционерное общество "Кировская фармацевтическая фабрика"
  • Невирапин
    таблетки, 200 мг (original in Russian, GRLS)
    ЛП-№(013348)-(РГ-RU)
    Общество с ограниченной ответственностью "Атолл" (ООО "Атолл")
  • Невирапин
    субстанция-порошок, ~, 100 г (original in Russian, GRLS)
    ФС-000118
    Хетеро Лабс Лимитед
All products in this country (22)
US 9
  • NEVIRAPINE
    TABLET · NEVIRAPINE 200 mg/1
    42571-131
    Micro Labs Limited
  • NEVIRAPINE
    TABLET, EXTENDED RELEASE · NEVIRAPINE 400 mg/1
    33342-238
    Macleods Pharmaceuticals Limited
  • Nevirapine
    TABLET, EXTENDED RELEASE · NEVIRAPINE 400 mg/1
    0378-4890
    Mylan Pharmaceuticals Inc.
  • Nevirapine
    TABLET · NEVIRAPINE 200 mg/1
    65162-209
    Amneal Pharmaceuticals LLC
  • Nevirapine
    SUSPENSION · NEVIRAPINE HEMIHYDRATE 50 mg/5mL
    65862-057
    Aurobindo Pharma Limited
All products in this country (9)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-4119-797e-9176-5c31ce55dce7,01a120c3-787b-7aa3-a94d-12bc566c52dc,01a120c3-ce5d-7357-bea2-4d3b048b89d2,01a120c3-d4ac-7964-b6ce-9f4e96cb496a,01a120c4-2981-711c-8b2a-ab4c2fb96293;count=13 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-b40c-7376-a48e-1e9612d9362a,01a1208d-7847-733d-92be-3e9623aa5fd9,01a12093-6797-795c-82fb-2fb72fa7d033,01a12095-935d-7efe-99ec-a74ab9f2974c,01a12096-e901-7d6a-945d-8534cec5782b;count=9 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
EMEA/H/C/001119
Registration status
Withdrawn
ATC code
J05AG01
Sources
  • product · EMA · EMEA/H/C/001119 · Verified 2026-10-09
  • registration_status · EMA · EMEA/H/C/001119 · Verified 2026-10-09
  • ingredients.0 · EMA · EMEA/H/C/001119 · Verified 2026-10-09