United States · FDA National Drug Code directory
Dye Free 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
- 0363-0438_fe9d1e9a-a785-46b5-9ef3-fae3e558bb23
- Product NDC
- 0363-0438
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Walgreen Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990301
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (0363-0438-32) / 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 0363-0438-32
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0438-98) · 0363-0438-98
- 1 BOTTLE, PLASTIC in 1 CARTON (0363-0438-99) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 0363-0438-99
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 →