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SULINDAC

Active substance: sulindac

TABLET · SULINDAC 200 mg/1

United StatesActive

Marketing holder: PuraCap Laboratories LLC dba Blu Pharmaceuticals

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
EU 1
  • Flynpovi
    eflornithine hydrochloride, sulindac
    EMEA/H/C/005043
    Cancer Prevention Pharma (Ireland) Limited
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-3264-7537-a145-f7297c4a81c2,01a1208c-4d70-7a8f-a9fc-e84c376f39a7,01a1208d-17b8-70e7-bf86-afe69654be71,01a1208d-4378-7a80-9c95-8f74595a6c41,01a12090-e8ae-7818-8b44-5a83710fe5b9;count=14 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
24658-771
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 24658-771 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 24658-771 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 24658-771 · Verified 2026-10-09 · open in source