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
- 70518-0761_557ab103-963d-f7b5-e063-6394a90aac5b
- Product NDC
- 70518-0761
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171006
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-0) · 70518-0761-0
- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-1) · 70518-0761-1
- 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-2) · 70518-0761-2
- 21 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-3) · 70518-0761-3
- 15 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-4) · 70518-0761-4
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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