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
- 42681-0061_4db585fe-bff2-f8a1-e063-6294a90acb3a
- Product NDC
- 42681-0061
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- IBUPROFEN AND DIPHENHYDRAMINE HCL
- Labeler
- Whole Foods Market, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260501
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (42681-0061-1) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 42681-0061-1
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 →