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
- 67060-001_feb250d0-cddb-448d-b08d-00a0fc091055
- Product NDC
- 67060-001
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN 200MG
- Labeler
- ADVANCED FIRST AID, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150409
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 250 PACKET in 1 CARTON (67060-001-67) / 2 TABLET, FILM COATED in 1 PACKET · 67060-001-67
- 100 PACKET in 1 CARTON (67060-001-68) / 2 TABLET, FILM COATED in 1 PACKET · 67060-001-68
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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