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
- 58602-802_5e6a6cce-b25c-4d6c-9d58-b4db175c6f8e
- Product NDC
- 58602-802
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- Aurohealth LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171108
- 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 (58602-802-07) / 24 TABLET in 1 BOTTLE · 58602-802-07
- 1 BOTTLE in 1 CARTON (58602-802-14) / 50 TABLET in 1 BOTTLE · 58602-802-14
- 1 BOTTLE in 1 CARTON (58602-802-21) / 100 TABLET in 1 BOTTLE · 58602-802-21
- 1 BOTTLE in 1 CARTON (58602-802-29) / 150 TABLET in 1 BOTTLE · 58602-802-29
- 200 TABLET in 1 BOTTLE (58602-802-34) · 58602-802-34
- 300 TABLET in 1 BOTTLE (58602-802-38) · 58602-802-38
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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