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
- 57896-941_08f1bde2-f476-2d2f-e063-6294a90a6f93
- Product NDC
- 57896-941
- Form
- TABLET, FILM COATED
- Composition / generic term
- ibuprofen
- Labeler
- Geri-Care Pharmaceutical Corp
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040101
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (57896-941-01) · 57896-941-01
- 50 TABLET, FILM COATED in 1 BOTTLE (57896-941-05) · 57896-941-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (57896-941-10) · 57896-941-10
- 1 BOTTLE in 1 CARTON (57896-941-20) / 200 TABLET, FILM COATED in 1 BOTTLE · 57896-941-20
- 500 TABLET, FILM COATED in 1 BOTTLE (57896-941-50) · 57896-941-50
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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