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
- 71335-1206_cd0c9ccd-cf1d-46f9-9598-58b43ebcb239
- Product NDC
- 71335-1206
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180824
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 84 TABLET, FILM COATED in 1 BOTTLE (71335-1206-0) · 71335-1206-0
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1206-1) · 71335-1206-1
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-1206-2) · 71335-1206-2
- 40 TABLET, FILM COATED in 1 BOTTLE (71335-1206-3) · 71335-1206-3
- 21 TABLET, FILM COATED in 1 BOTTLE (71335-1206-4) · 71335-1206-4
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1206-5) · 71335-1206-5
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1206-6) · 71335-1206-6
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1206-7) · 71335-1206-7
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-1206-8) · 71335-1206-8
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1206-9) · 71335-1206-9
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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