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
- 50090-7288_73a943cb-930a-4bed-9fa6-f818926e2e7a
- Product NDC
- 50090-7288
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240523
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (50090-7288-0) · 50090-7288-0
- 16 TABLET, FILM COATED in 1 BOTTLE (50090-7288-2) · 50090-7288-2
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-7288-3) · 50090-7288-3
- 60 TABLET, FILM COATED in 1 BOTTLE (50090-7288-4) · 50090-7288-4
- 100 TABLET, FILM COATED in 1 BOTTLE (50090-7288-5) · 50090-7288-5
- 40 TABLET, FILM COATED in 1 BOTTLE (50090-7288-7) · 50090-7288-7
- 20 TABLET, FILM COATED in 1 BOTTLE (50090-7288-8) · 50090-7288-8
- 24 TABLET, FILM COATED in 1 BOTTLE (50090-7288-9) · 50090-7288-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →