United States · FDA National Drug Code directory
IBUPROFEN Immediate Release
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
- 59556-857_429d1cf2-cd25-4622-a9f9-60cede85df5f
- Product NDC
- 59556-857
- Form
- TABLET, COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- Strides Pharma Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220318
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10000 TABLET, COATED in 1 BAG (59556-857-42) · 59556-857-42
- 30000 TABLET, COATED in 1 BAG (59556-857-43) · 59556-857-43
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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