United States · FDA National Drug Code directory
Ibuprofen PM
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
- 0363-0050_2e8f3546-0aa7-4f2d-a201-037e01bae76a
- Product NDC
- 0363-0050
- Form
- TABLET, FILM COATED
- Composition / generic term
- diphenhydramine citrate, ibuprofen
- Labeler
- Walgreen Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090219
- Source listing expiry
- 20261231
Source-listed ingredients
- DIPHENHYDRAMINE CITRATE — 38 mg/1
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (0363-0050-27) / 80 TABLET, FILM COATED in 1 BOTTLE · 0363-0050-27
- 1 BOTTLE in 1 CARTON (0363-0050-58) / 40 TABLET, FILM COATED in 1 BOTTLE · 0363-0050-58
- 1 BOTTLE in 1 CARTON (0363-0050-60) / 20 TABLET, FILM COATED in 1 BOTTLE · 0363-0050-60
- 1 BOTTLE in 1 CARTON (0363-0050-76) / 120 TABLET, FILM COATED in 1 BOTTLE · 0363-0050-76
- 200 TABLET, FILM COATED in 1 BOTTLE (0363-0050-82) · 0363-0050-82
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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