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
- 41226-601_3f89772f-94d8-4e14-e063-6294a90a769b
- Product NDC
- 41226-601
- Form
- TABLET, COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- Kroger Company
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20210410
- 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 (41226-601-01) / 100 TABLET, COATED in 1 BOTTLE · 41226-601-01
- 1 BOTTLE in 1 CARTON (41226-601-05) / 50 TABLET, COATED in 1 BOTTLE · 41226-601-05
- 2 BOTTLE in 1 PACKAGE, COMBINATION (41226-601-10) / 500 TABLET, COATED in 1 BOTTLE (41226-601-53) · 41226-601-10
- 200 TABLET, COATED in 1 BOTTLE (41226-601-20) · 41226-601-20
- 250 TABLET, COATED in 1 BOTTLE (41226-601-25) · 41226-601-25
- 1 BOTTLE in 1 CARTON (41226-601-42) / 24 TABLET, COATED in 1 BOTTLE · 41226-601-42
- 500 TABLET, COATED in 1 BOTTLE (41226-601-53) · 41226-601-53
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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