United States · FDA National Drug Code directory
equaline 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
- 41163-647_4468b48a-3b80-4b37-b3bb-b521f351c618
- Product NDC
- 41163-647
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- United Natural Foods, Inc. dba UNFI
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040817
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (41163-647-71) / 50 TABLET, FILM COATED in 1 BOTTLE · 41163-647-71
- 1 BOTTLE in 1 CARTON (41163-647-78) / 100 TABLET, FILM COATED in 1 BOTTLE · 41163-647-78
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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