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
- 37808-699_5c1c8f93-720d-4ae8-bab2-5933f691fff1
- Product NDC
- 37808-699
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Ibuprofen
- Labeler
- H E B
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180331
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 BOX (37808-699-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 37808-699-20
- 300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (37808-699-30) · 37808-699-30
- 1 BOTTLE, PLASTIC in 1 BOX (37808-699-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 37808-699-40
- 1 BOTTLE, PLASTIC in 1 BOX (37808-699-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 37808-699-80
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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