United States · FDA National Drug Code directory
Acetaminophen and Ibuprofen
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
- 50844-598_48c90e4c-f0be-4d69-9d89-a6ace79f51b0
- Product NDC
- 50844-598
- Form
- TABLET, FILM COATED
- Composition / generic term
- Acetaminophen, Ibuprofen
- Labeler
- L.N.K. International, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260910
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAMINOPHEN — 250 mg/1
- IBUPROFEN — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-598-14) · 50844-598-14
- 1 BOTTLE, PLASTIC in 1 CARTON (50844-598-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-598-19
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 →