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
- 71335-1517_840d6421-5e3e-4933-84fb-e5676439b9a0
- Product NDC
- 71335-1517
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151230
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1) · 71335-1517-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1517-2) · 71335-1517-2
- 40 TABLET, FILM COATED in 1 BOTTLE (71335-1517-3) · 71335-1517-3
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1517-4) · 71335-1517-4
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1517-5) · 71335-1517-5
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-1517-6) · 71335-1517-6
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1517-7) · 71335-1517-7
- 21 TABLET, FILM COATED in 1 BOTTLE (71335-1517-8) · 71335-1517-8
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-1517-9) · 71335-1517-9
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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