United States · FDA National Drug Code directory

ibuprofen pm

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: 56062-050_726da18f-09ef-4378-bdb3-abd5d6513642
Product NDC: 56062-050
Form: TABLET, FILM COATED
Composition / generic term: diphenhydramine citrate, ibuprofen
Labeler: Publix Super Markets Inc
Marketing category: ANDA
Marketing start / end (source format): 20110915
Source listing expiry: 20261231

Source-listed ingredients

DIPHENHYDRAMINE CITRATE — 38 mg/1
IBUPROFEN — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (56062-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE · 56062-050-58

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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