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
- 50090-5446_3d7a2f69-acb6-4040-9cd4-519fa5a20067
- Product NDC
- 50090-5446
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200508
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (50090-5446-0) · 50090-5446-0
- 30 TABLET in 1 BOTTLE (50090-5446-2) · 50090-5446-2
- 45 TABLET in 1 BOTTLE (50090-5446-3) · 50090-5446-3
- 60 TABLET in 1 BOTTLE (50090-5446-4) · 50090-5446-4
- 100 TABLET in 1 BOTTLE (50090-5446-5) · 50090-5446-5
- 21 TABLET in 1 BOTTLE (50090-5446-7) · 50090-5446-7
- 12 TABLET in 1 BOTTLE (50090-5446-8) · 50090-5446-8
- 40 TABLET in 1 BOTTLE (50090-5446-9) · 50090-5446-9
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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