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
- 63868-773_c2bb3799-d8e4-4130-973e-9b1b0d7db096
- Product NDC
- 63868-773
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19880524
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63868-773-05) · 63868-773-05
- 1 BOTTLE, PLASTIC in 1 CARTON (63868-773-10) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 63868-773-10
- 1 BOTTLE, PLASTIC in 1 CARTON (63868-773-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 63868-773-24
- 1 BOTTLE, PLASTIC in 1 CARTON (63868-773-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 63868-773-50
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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