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
- 72288-640_b1fa19b4-76fa-4f0b-82b4-b8d55a663c1f
- Product NDC
- 72288-640
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- ibuprofen
- Labeler
- Amazon.com Services LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260701
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (72288-640-06) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE (72288-640-00) · 72288-640-06
- 300 CAPSULE, LIQUID FILLED in 1 BOTTLE (72288-640-87) · 72288-640-87
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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