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
- 11822-6604_2ceba01b-fad3-4aca-8df7-84bc6372c96e
- Product NDC
- 11822-6604
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Rite Aid Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200904 / 20270228
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (11822-6604-2) / 50 TABLET, FILM COATED in 1 BOTTLE · 11822-6604-2
- 1 BOTTLE in 1 CARTON (11822-6604-3) / 100 TABLET, FILM COATED in 1 BOTTLE · 11822-6604-3
- 500 TABLET, FILM COATED in 1 BOTTLE (11822-6604-4) · 11822-6604-4
- 1 BOTTLE in 1 CARTON (11822-6604-5) / 24 TABLET, FILM COATED in 1 BOTTLE · 11822-6604-5
- 1 BOTTLE in 1 CARTON (11822-6604-6) / 200 TABLET, FILM COATED in 1 BOTTLE · 11822-6604-6
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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