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
- 54348-830_eaa5b55d-10b0-aab9-e053-2995a90a05d7
- Product NDC
- 54348-830
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- PharmPak, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190711
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 BOX (54348-830-00) / 1 TABLET, FILM COATED in 1 BOTTLE · 54348-830-00
- 1 BOTTLE in 1 BOX (54348-830-02) / 2 TABLET, FILM COATED in 1 BOTTLE · 54348-830-02
- 1 BOTTLE in 1 BOX (54348-830-08) / 8 TABLET, FILM COATED in 1 BOTTLE · 54348-830-08
- 1 BOTTLE in 1 BOX (54348-830-10) / 10 TABLET, FILM COATED in 1 BOTTLE · 54348-830-10
- 1 BOTTLE in 1 BOX (54348-830-12) / 12 TABLET, FILM COATED in 1 BOTTLE · 54348-830-12
- 1 BOTTLE in 1 BOX (54348-830-20) / 20 TABLET, FILM COATED in 1 BOTTLE · 54348-830-20
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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