United States · FDA National Drug Code directory
Ibuprofen 200
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
- 0363-0393_d6695f02-fda6-4dfa-a57f-19b50e264bcd
- Product NDC
- 0363-0393
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Walgreen Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990301 / 20261031
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0393-20) · 0363-0393-20
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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