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Repaglinide

Active substance: repaglinide

TABLET · REPAGLINIDE 1 mg/1

United StatesActive

Marketing holder: Bryant Ranch Prepack

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 7
  • Диаглинид
    таблетки, 1 мг (original in Russian, GRLS)
    ЛП-№(003132)-(РГ-RU)
    Акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (АО "АКРИХИН")
  • Диаглинид
    таблетки, 1 мг (original in Russian, GRLS)
    ЛП-001261
    Акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (АО "АКРИХИН")
  • Иглинид
    таблетки, 1 мг (original in Russian, GRLS)
    ЛП-№(000676)-(РГ-RU)
    Общество с ограниченной ответственностью "Фармасинтез-Тюмень" (ООО "Фармасинтез-Тюмень")
  • Репаглинид
    субстанция-порошок, ~, 50 кг (original in Russian, GRLS)
    ЛСР-001140/10
    Сан Фармасьютикал Индастриз Лтд
  • Репаглинид
    субстанция, ~, 15 кг (original in Russian, GRLS)
    ФС-000781
    Фармацевтический завод "ПОЛЬФАРМА" АО
All products in this country (7)
EU 7
  • Enyglid
    repaglinide
    EMEA/H/C/001065
    Krka, d.d., Novo mesto
  • NovoNorm
    repaglinide
    EMEA/H/C/000187
    Novo Nordisk A/S
  • Prandin
    repaglinide
    EMEA/H/C/000362
    Novo Nordisk A/S
  • Repaglinide Krka
    repaglinide
    EMEA/H/C/001066
    Krka, d.d., Novo mesto
  • Repaglinide Sun
    repaglinide
    EMEA/H/C/001145
    Sun Pharmaceutical Industries B.V.
All products in this country (7)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-38ab-7963-a675-473937f132a7,01a120c3-515f-73d7-ada2-47756de960d7,01a120c4-de6d-76ef-9ebf-3f644517e322,01a120c5-2028-7114-8cb7-ee979f79fb6f,01a120c5-a416-7a8f-8a92-55a06d61e485;count=5 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-299c-7f13-87ac-4eef0aede2c0,01a1208c-8463-7ce0-a68d-7589a5992c2a,01a1208d-07d7-75db-9888-3f410d354034,01a1208d-7ae7-72a7-98da-8eab896d5e9b,01a1208d-bbab-78de-a68f-a548236f8e5f;count=20 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
72162-2558
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 72162-2558 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 72162-2558 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 72162-2558 · Verified 2026-10-09 · open in source