United States · FDA National Drug Code directory
care one 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
- 41520-604_ec4746b3-2707-40c5-bb70-58a42f46c249
- Product NDC
- 41520-604
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- American Sales Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040413
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (41520-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE · 41520-604-71
- 1 BOTTLE in 1 CARTON (41520-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE · 41520-604-78
- 250 TABLET, FILM COATED in 1 BOTTLE (41520-604-85) · 41520-604-85
- 500 TABLET, FILM COATED in 1 BOTTLE (41520-604-90) · 41520-604-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (41520-604-93) · 41520-604-93
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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