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
- 72789-364_570ebcac-82b1-04d2-e063-6294a90a9313
- Product NDC
- 72789-364
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151221
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-06) · 72789-364-06
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-10) · 72789-364-10
- 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-15) · 72789-364-15
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-20) · 72789-364-20
- 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-21) · 72789-364-21
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-30) · 72789-364-30
- 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-40) · 72789-364-40
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-60) · 72789-364-60
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-90) · 72789-364-90
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-364-93) · 72789-364-93
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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