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
- 42507-647_540e3bdd-bc24-4016-a8e3-ef9d0af384ea
- Product NDC
- 42507-647
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- HyVee Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19890715
- 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 (42507-647-62) / 24 TABLET, FILM COATED in 1 BOTTLE · 42507-647-62
- 1 BOTTLE in 1 CARTON (42507-647-71) / 50 TABLET, FILM COATED in 1 BOTTLE (42507-647-50) · 42507-647-71
- 1 BOTTLE in 1 CARTON (42507-647-78) / 100 TABLET, FILM COATED in 1 BOTTLE (42507-647-00) · 42507-647-78
- 500 TABLET, FILM COATED in 1 BOTTLE (42507-647-90) · 42507-647-90
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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