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Probenecid

Active substance: probenecid

TABLET · PROBENECID 500 mg/1

United StatesActive

Marketing holder: REMEDYREPACK INC.

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-298f-718d-97e1-ff030d84f313,01a1208e-dd33-7b62-a80c-1f8b576f2b6a,01a12091-6f8f-7c42-858d-ff5dd27ae07e,01a12092-a282-7588-a076-ee15f9db508f,01a12097-db31-7a52-acfc-22cee32051f4;count=7 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
70518-4649
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 70518-4649 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 70518-4649 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 70518-4649 · Verified 2026-10-09 · open in source