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
- 62207-354_44dee7dd-17ff-8faa-e063-6294a90a6712
- Product NDC
- 62207-354
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Granules India Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150921
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TABLET, FILM COATED in 1 BOTTLE (62207-354-42) · 62207-354-42
- 100 TABLET, FILM COATED in 1 BOTTLE (62207-354-43) · 62207-354-43
- 500 TABLET, FILM COATED in 1 BOTTLE (62207-354-47) · 62207-354-47
- 1000 TABLET, FILM COATED in 1 BOTTLE (62207-354-49) · 62207-354-49
- 30 TABLET, FILM COATED in 1 BOTTLE (62207-354-54) · 62207-354-54
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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