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
- 79903-186_fec3c891-139c-4171-8c7a-dfe802e7e04d
- Product NDC
- 79903-186
- Form
- TABLET, COATED
- Composition / generic term
- Diphenhydramine Citrate, Ibuprofen
- Labeler
- WALMART INC. (see also Equate)
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240608 / 20271228
Source-listed ingredients
- IBUPROFEN — 200 mg/1
- DIPHENHYDRAMINE CITRATE — 38 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 BOX (79903-186-20) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC · 79903-186-20
- 1 BOTTLE, PLASTIC in 1 BOX (79903-186-80) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC · 79903-186-80
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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