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
- 0363-9612_13b22280-b329-93b4-e063-6394a90a12f9
- Product NDC
- 0363-9612
- Form
- TABLET
- Composition / generic term
- IBUPROFEN
- Labeler
- WALGREENS
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181211
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (0363-9612-01) · 0363-9612-01
- 50 TABLET in 1 BOTTLE, PLASTIC (0363-9612-05) · 0363-9612-05
- 225 TABLET in 1 BOTTLE, PLASTIC (0363-9612-26) · 0363-9612-26
- 500 TABLET in 1 BOTTLE, PLASTIC (0363-9612-50) · 0363-9612-50
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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