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
- 11822-0050_4b815346-969e-4f5a-af95-09d3c984b36c
- Product NDC
- 11822-0050
- Form
- TABLET, FILM COATED
- Composition / generic term
- Diphenhydramine Citrate, Ibuprofen
- Labeler
- Rite Aid Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090319 / 20261031
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 (11822-0050-3) / 20 TABLET, FILM COATED in 1 BOTTLE · 11822-0050-3
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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