United States · FDA National Drug Code directory
CELECOXIB
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
- 60290-018_499a5e50-a378-7aff-e063-6294a90adc85
- Product NDC
- 60290-018
- Form
- CAPSULE
- Composition / generic term
- CELECOXIB
- Labeler
- Umedica Laboratories USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260215
- Source listing expiry
- 20271231
Source-listed ingredients
- CELECOXIB — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BLISTER PACK (60290-018-01) · 60290-018-01
- 100 CAPSULE in 1 BOTTLE (60290-018-02) · 60290-018-02
- 500 CAPSULE in 1 BOTTLE (60290-018-03) · 60290-018-03
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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