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
- 67751-120_f70c1b68-61c9-b333-e053-6294a90aadaa
- Product NDC
- 67751-120
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- Navajo Manufacturing Company Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20160922
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 CARTON (67751-120-01) / 2 TABLET, FILM COATED in 1 POUCH · 67751-120-01
- 2 POUCH in 1 CARTON (67751-120-02) / 2 TABLET, FILM COATED in 1 POUCH · 67751-120-02
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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