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
- 21130-623_fe3393ad-a18f-40cd-abb4-77fb876bd7aa
- Product NDC
- 21130-623
- Form
- TABLET, FILM COATED
- Composition / generic term
- diphenhydramine citrate, ibuprofen
- Labeler
- Safeway
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251229
- Source listing expiry
- 20271231
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 (21130-623-76) / 120 TABLET, FILM COATED in 1 BOTTLE · 21130-623-76
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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