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
- 76282-714_bc309c22-f359-42b1-86db-3970a5d53bc4
- Product NDC
- 76282-714
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- EXELAN PHARMACEUTICALS, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220310
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (76282-714-10) · 76282-714-10
- 30 TABLET, FILM COATED in 1 BOTTLE (76282-714-30) · 76282-714-30
- 100 BLISTER PACK in 1 CARTON (76282-714-46) / 10 TABLET, FILM COATED in 1 BLISTER PACK (76282-714-45) · 76282-714-46
- 500 TABLET, FILM COATED in 1 BOTTLE (76282-714-50) · 76282-714-50
- 1000 TABLET, FILM COATED in 1 BOTTLE (76282-714-55) · 76282-714-55
- 90 TABLET, FILM COATED in 1 BOTTLE (76282-714-90) · 76282-714-90
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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