United States · FDA National Drug Code directory
equaline 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
- 41163-050_d06f41f5-6ade-4964-a941-d8fc41a39529
- Product NDC
- 41163-050
- Form
- TABLET, FILM COATED
- Composition / generic term
- diphenhydramine citrate, ibuprofen
- Labeler
- United Natural Foods, Inc. dba UNFI
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090302
- 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 (41163-050-27) / 80 TABLET, FILM COATED in 1 BOTTLE · 41163-050-27
- 1 BOTTLE in 1 CARTON (41163-050-58) / 40 TABLET, FILM COATED in 1 BOTTLE · 41163-050-58
- 1 BOTTLE in 1 CARTON (41163-050-60) / 20 TABLET, FILM COATED in 1 BOTTLE · 41163-050-60
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 →