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
- 70010-067_5125d89b-4fd5-b823-e063-6394a90a1eff
- Product NDC
- 70010-067
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Granules Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260218
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (70010-067-01) · 70010-067-01
- 30 TABLET, FILM COATED in 1 BOTTLE (70010-067-03) · 70010-067-03
- 500 TABLET, FILM COATED in 1 BOTTLE (70010-067-05) · 70010-067-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (70010-067-10) · 70010-067-10
- 50 TABLET, FILM COATED in 1 BOTTLE (70010-067-50) · 70010-067-50
- 6 BLISTER PACK in 1 CARTON (70010-067-81) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 70010-067-81
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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