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
- 50090-7283_2f42bfa3-a3a5-40fd-bbca-973a984d4d2c
- Product NDC
- 50090-7283
- 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 — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (50090-7283-0) · 50090-7283-0
- 15 TABLET, FILM COATED in 1 BOTTLE (50090-7283-1) · 50090-7283-1
- 30 TABLET, FILM COATED in 1 BOTTLE (50090-7283-2) · 50090-7283-2
- 45 TABLET, FILM COATED in 1 BOTTLE (50090-7283-3) · 50090-7283-3
- 60 TABLET, FILM COATED in 1 BOTTLE (50090-7283-4) · 50090-7283-4
- 100 TABLET, FILM COATED in 1 BOTTLE (50090-7283-5) · 50090-7283-5
- 21 TABLET, FILM COATED in 1 BOTTLE (50090-7283-7) · 50090-7283-7
- 12 TABLET, FILM COATED in 1 BOTTLE (50090-7283-8) · 50090-7283-8
- 40 TABLET, FILM COATED in 1 BOTTLE (50090-7283-9) · 50090-7283-9
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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