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
- 60760-597_51cca64c-9a12-9785-e063-6394a90af9be
- Product NDC
- 60760-597
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190502
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-20) · 60760-597-20
- 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-28) · 60760-597-28
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-30) · 60760-597-30
- 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-40) · 60760-597-40
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-60) · 60760-597-60
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-597-90) · 60760-597-90
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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