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
- 11788-009_3be8b50a-af8c-44d9-8c3a-02cb83eaae82
- Product NDC
- 11788-009
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- AiPing Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251215
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (11788-009-01) · 11788-009-01
- 500 TABLET, FILM COATED in 1 BOTTLE (11788-009-05) · 11788-009-05
- 1250 TABLET, FILM COATED in 1 BOTTLE (11788-009-20) · 11788-009-20
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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