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Acetaminophen 250 mg and Ibuprofen 125 mg

Active substance: ACETAMINOPHEN, IBUPROFEN

TABLET · ACETAMINOPHEN 250 mg/1, IBUPROFEN 125 mg/1

United StatesActive

Marketing holder: Sun Pharmaceutical Industries, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • ACETAMINOPHEN · 250 mg/1
  • IBUPROFEN · 125 mg/1
Registration
Registration number
51672-4258
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 51672-4258 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 51672-4258 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 51672-4258 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 51672-4258 · Verified 2026-10-09 · open in source