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
- 71205-357_c18cb763-af0c-4cc2-b7df-520835c91884
- Product NDC
- 71205-357
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180920
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, FILM COATED in 1 BOTTLE (71205-357-06) · 71205-357-06
- 24 TABLET, FILM COATED in 1 BOTTLE (71205-357-24) · 71205-357-24
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-357-30) · 71205-357-30
- 50 TABLET, FILM COATED in 1 BOTTLE (71205-357-50) · 71205-357-50
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-357-60) · 71205-357-60
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-357-90) · 71205-357-90
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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