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Oxaprozin

Active substance: oxaprozin

TABLET · OXAPROZIN 600 mg/1

United StatesActive

Marketing holder: Amneal Pharmaceuticals NY LLC

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-3872-7261-b6e4-8e8b9b0642b8,01a1208c-b62a-72ee-b5f5-d683848e8d1f,01a1208d-4201-7cb4-a777-2b8d226e713a,01a1208d-5d04-7458-b3bb-5e2567d33a1b,01a12092-7c78-78af-bc4b-5c752ef3b360;count=10 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
69238-1120
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 69238-1120 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 69238-1120 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 69238-1120 · Verified 2026-10-09 · open in source