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
- 68071-4009_1d7a1de1-b173-b168-e063-6294a90a878c
- Product NDC
- 68071-4009
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151230
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET, FILM COATED in 1 BOTTLE (68071-4009-1) · 68071-4009-1
- 20 TABLET, FILM COATED in 1 BOTTLE (68071-4009-2) · 68071-4009-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68071-4009-3) · 68071-4009-3
- 40 TABLET, FILM COATED in 1 BOTTLE (68071-4009-4) · 68071-4009-4
- 50 TABLET, FILM COATED in 1 BOTTLE (68071-4009-5) · 68071-4009-5
- 60 TABLET, FILM COATED in 1 BOTTLE (68071-4009-6) · 68071-4009-6
- 15 TABLET, FILM COATED in 1 BOTTLE (68071-4009-7) · 68071-4009-7
- 90 TABLET, FILM COATED in 1 BOTTLE (68071-4009-9) · 68071-4009-9
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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