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
- 72476-365_465138e1-6e59-a9e1-e063-6294a90ae8df
- Product NDC
- 72476-365
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- RETAIL BUSINESS SERVICES,LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200726
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TABLET in 1 BOTTLE (72476-365-05) · 72476-365-05
- 100 TABLET in 1 BOTTLE (72476-365-10) · 72476-365-10
- 200 TABLET in 1 BOTTLE (72476-365-20) · 72476-365-20
- 24 TABLET in 1 BOTTLE (72476-365-24) · 72476-365-24
- 500 TABLET in 1 BOTTLE (72476-365-50) · 72476-365-50
- 1000 TABLET in 1 BOTTLE (72476-365-99) · 72476-365-99
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 →