United States · FDA National Drug Code directory

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: 72789-186_34178401-0edc-512f-e063-6294a90ab88a
Product NDC: 72789-186
Form: TABLET, FILM COATED
Composition / generic term: Ibuprofen
Labeler: PD-Rx Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20200821
Source listing expiry: 20261231

Source-listed ingredients

IBUPROFEN — 800 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-30) · 72789-186-30
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-60) · 72789-186-60
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-82) · 72789-186-82
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-186-90) · 72789-186-90

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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