United States · FDA National Drug Code directory

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
0363-0221_f0e93c45-051d-7362-e053-2a95a90a0cb2
Product NDC
0363-0221
Form
CAPSULE, LIQUID FILLED
Composition / generic term
Ibuprofen
Labeler
WALGREEN COMPANY
Marketing category
ANDA
Marketing start / end (source format)
20190802
Source listing expiry
20261231

Source-listed ingredients

  • IBUPROFEN — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (0363-0221-11) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE · 0363-0221-11
  • 1 BOTTLE in 1 CARTON (0363-0221-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE · 0363-0221-15
  • 1 BOTTLE in 1 CARTON (0363-0221-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE · 0363-0221-78
  • 1 BOTTLE in 1 CARTON (0363-0221-79) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE · 0363-0221-79
  • 300 CAPSULE, LIQUID FILLED in 1 BOTTLE (0363-0221-83) · 0363-0221-83

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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