United States · FDA National Drug Code directory
dual pain reliever
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
- 0363-5220_eb14452c-519f-4a6b-866a-4a7f15f22f57
- Product NDC
- 0363-5220
- Form
- TABLET, FILM COATED
- Composition / generic term
- Acetaminophen, Ibuprofen
- Labeler
- Walgreen Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230310
- 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
- 1 BOTTLE in 1 CARTON (0363-5220-01) / 216 TABLET, FILM COATED in 1 BOTTLE · 0363-5220-01
- 1 BOTTLE in 1 CARTON (0363-5220-16) / 144 TABLET, FILM COATED in 1 BOTTLE · 0363-5220-16
- 1 BOTTLE in 1 CARTON (0363-5220-23) / 72 TABLET, FILM COATED in 1 BOTTLE · 0363-5220-23
- 1 BOTTLE in 1 CARTON (0363-5220-68) / 36 TABLET, FILM COATED in 1 BOTTLE · 0363-5220-68
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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