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
- 71335-3121_00e9051f-6b68-4770-9007-e9fb67a8da38
- Product NDC
- 71335-3121
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240523
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET, FILM COATED in 1 BOTTLE (71335-3121-0) · 71335-3121-0
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-3121-1) · 71335-3121-1
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-3121-2) · 71335-3121-2
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-3121-3) · 71335-3121-3
- 40 TABLET, FILM COATED in 1 BOTTLE (71335-3121-4) · 71335-3121-4
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-3121-5) · 71335-3121-5
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-3121-6) · 71335-3121-6
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-3121-7) · 71335-3121-7
- 50 TABLET, FILM COATED in 1 BOTTLE (71335-3121-8) · 71335-3121-8
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-3121-9) · 71335-3121-9
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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