United States · FDA National Drug Code directory
Motrin IB
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
- 73097-028_56846774-8414-c306-e063-6394a90a2be8
- Product NDC
- 73097-028
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- Savings Distributors LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20260101
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 CARTON (73097-028-02) / 2 TABLET, FILM COATED in 1 POUCH · 73097-028-02
- 20 POUCH in 1 CARTON (73097-028-40) / 2 TABLET, FILM COATED in 1 POUCH · 73097-028-40
- 25 POUCH in 1 CARTON (73097-028-50) / 2 TABLET, FILM COATED in 1 POUCH · 73097-028-50
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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