United States · FDA National Drug Code directory

Acetaminophen and Ibuprofen

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: 69452-394_45c4da17-7d0d-421b-e063-6294a90a6a2e
Product NDC: 69452-394
Form: TABLET, FILM COATED
Composition / generic term: Acetaminophen and Ibuprofen
Labeler: Bionpharma Inc.
Marketing category: ANDA
Marketing start / end (source format): 20230908
Source listing expiry: 20261231

Source-listed ingredients

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

These values do not establish equivalence or a dose recommendation.

Packages

216 TABLET, FILM COATED in 1 BOTTLE (69452-394-64) · 69452-394-64
400 TABLET, FILM COATED in 1 BOTTLE (69452-394-81) · 69452-394-81

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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