United States · FDA National Drug Code directory
Uline 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
- 69790-609_3e5d77e9-9142-41d7-e063-6294a90a365e
- Product NDC
- 69790-609
- Form
- TABLET, COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Uline
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220404
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 PACKET in 1 BOX (69790-609-33) / 2 TABLET, COATED in 1 PACKET · 69790-609-33
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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