United States · FDA National Drug Code directory

equate dual pain reliever

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
79903-243_f4e59631-e3b3-4ef2-b164-f23f856b39c0
Product NDC
79903-243
Form
TABLET, FILM COATED
Composition / generic term
Acetaminophen, Ibuprofen
Labeler
WALMART INC.
Marketing category
ANDA
Marketing start / end (source format)
20250311
Source listing expiry
20261231

Source-listed ingredients

  • ACETAMINOPHEN — 250 mg/1
  • IBUPROFEN — 125 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (79903-243-36) / 36 TABLET, FILM COATED in 1 BOTTLE · 79903-243-36
  • 1 BOTTLE in 1 CARTON (79903-243-72) / 72 TABLET, FILM COATED in 1 BOTTLE · 79903-243-72

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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