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
68016-057_21afce91-afbe-4b38-a8a5-8775148835e8
Product NDC
68016-057
Form
CAPSULE, LIQUID FILLED
Composition / generic term
IBUPROFEN, DIPHENHYDRAMINE HCL
Labeler
Premier Value Alliance LLC
Marketing category
ANDA
Marketing start / end (source format)
20181025
Source listing expiry
20261231

Source-listed ingredients

  • IBUPROFEN — 200 mg/1
  • DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (68016-057-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE · 68016-057-40

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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