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
- 50332-0152_24531295-6ee5-4fcb-857b-50c3ea59e3c3
- Product NDC
- 50332-0152
- Form
- TABLET
- Composition / generic term
- ibuprofen
- Labeler
- HART Health
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20230101
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 PACKET in 1 BOX, UNIT-DOSE (50332-0152-4) / 2 TABLET in 1 PACKET · 50332-0152-4
- 125 PACKET in 1 BOX, UNIT-DOSE (50332-0152-7) / 2 TABLET in 1 PACKET · 50332-0152-7
- 250 PACKET in 1 BOX, UNIT-DOSE (50332-0152-8) / 2 TABLET in 1 PACKET · 50332-0152-8
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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